divendres, 30 de setembre del 2016

SQZ Biotech lands $16m in Series B for cell therapy tech

SQZ BiotechSQZ Biotech said today that it closed a $16 million Series B round to fund its preclinical cell therapy programs for oncology and other undisclosed diseases.

NanoDimension and Polaris Partners led the funding for the Boston, Mass.-based biotech startup.

SQZ said it developed a microchip that can open immune cell membranes temporarily and let proteins in that can trigger an immune response against cancer. The cell membrane is gently squeezed open and fragments of proteins from a tumor are taken up by B-cells.

The modified B-cells can train another class of immune cells known as T-cells, to hunt down and destroy the cancerous tissue, according to SQZ.

Other companies, like Novartis and Juno Therapeutics (NSDQ:JUNO), are attempting to use the body’s own immune system to destroy cancer cells by directly modifying T-cells. But it remains unclear how effective these treatments are in the long run and what kinds of cancers they can destroy.

SQZ entered into a $500 million partnership with Roche to address what they see as limitations in the cell therapy industry.

“SQZ has developed a simple, yet immensely powerful method to engineer cells,” NanoDimension’s Eric Moessinger, who joined the SQZ Board of Directors, said in prepared remarks. “I am thrilled to be a part of the SQZ team and look forward to contributing to the evolution of this innovative company.”

“The SQZ team has made remarkable progress,”  Polaris Partners venture partner and SQZ executive chair Amy Schulman added. “Soon the real promise of their cell re-engineering technology will be applied across a variety of applications to treat a broad range of ailments. I am confident this technology will represent a meaningful difference in people’s lives.”

SQZ also announced that it hired Kris Elverum as its Chief Business Officer. Elverum led US commercial model development for Novartis’ cell-therapy division, which was recently disbanded.

“Kris’ passion, leadership, and unique experience in cell therapy commercialization, strategy and M&A will be invaluable to SQZ at this time of growth for our company. We are very excited to have him on the team,” CEO Armon Sharei said.

The post SQZ Biotech lands $16m in Series B for cell therapy tech appeared first on MassDevice.



from MassDevice http://ift.tt/2dtE8YX

Philips spectral CT used on T-Rex spine

PhilipsRoyal Philips (NYSE:PHG) said today that researchers at the Naturalis museum in Leiden, Netherlands used its IQon CT scanner to closely examine the tail vertebrae of a 66 million year-old T-Rex named Trix.

Philips’ IQon scanner is the 1st detector-based spectral CT, using a dual-layer detector and advanced spectral reconstruction to compose a detailed image. Researchers from the museum hoped that the instrument could provide more detail than images from a traditional CT.

“The IQon filters out all the ‘noise,’ as it were, thereby providing a really good insight into the bone structure and how it is built up,” Naturalis paleontologist and dinosaur expert Anne Schulp said in prepared remarks. “It’s basically making the step from black and white movies to color. In this way, we are able to add depth to Trix’s medical records: we make the invisible visible. It’s just really hard to describe the sensation of finding something, seeing something that no one else has ever seen.”

Get the full story at our sister site, Medical Design & Outsourcing.

The post Philips spectral CT used on T-Rex spine appeared first on MassDevice.



from MassDevice http://ift.tt/2cGShpM

Delcath prices $1.3m offering

DelcathDelcath (NSDQ:DCTH) today priced a $1.28 million public offering of stock, with funding slated to support clinical trials and commercialization efforts.

The New York-based company said it plans to float 425,000 shares of its common stock at $3 per share. Investors in the round will also receive 0.35 warrants to purchase an additional share of common stock at $3 per share for up to 5 years.

Delcath expects to close the offering on October 5, 2016, according to a press release.

Funds from the round are expected to support general corporate purposes including clinical trial funding, product commercialization, regulatory approvals, research, capital expenditures and working capital, the company said.

Roth Capital Partners is acting as manager for the offering.

In June, Delcath said it inked a securities purchase agreement with an investor for $35 million in senior convertible notes and stock purchase warrants, expecting to bring in $32.2 million to support operations and ongoing clinical trials.

Of the $32.2 million in proceeds, Delcath said $3 million will be immediately available, with the remaining $29.2 million subject to a cash covenant restricting it and requiring it be held by control accounts of the company.

The post Delcath prices $1.3m offering appeared first on MassDevice.



from MassDevice http://ift.tt/2ddHLIh

MassDevice.com +5 | The top 5 medtech stories for September 30, 2016

plus5-node

Say hello to MassDevice +5, a bite-sized view of the top five medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 5 biggest and most influential stories from the day’s news to make sure you’re up to date on the headlines that continue to shape the medical device industry.

Get this in your inbox everyday by subscribing to our newsletters.

 

5. Sunshine Heart shifts focus to Aquadex FlexFlow system

MassDevice.com news

Sunshine Heart said today it will realign its strategy to focus on its recently acquired Aquadex FlexFlow system, designed to filter water and salt from patients with fluid overload due to renal failure.

The Eden Prairie, Minn.-based company acquired the system from Baxter for $5 million in August this year. It also said it will pause clinical evaluations of its neuromodulation tech and reduce cash burn to $80,000 per month in the 4th quarter of 2016. Read more


4. Mergers, IP, risk assessment among trends in medtech

MassDevice.com news

In 1995, the average time to a successful exit for a medical device startup was about 3 years, according to Rotational Medical CEO Martha Shadan. Now, Shadan said, it can range from 6 to 9 years and cost as much as $50 million. Shadan suggested that the increase in exit time is probably due to risk associated with investing in medtech and a lack of venture capitalists.

“This is a real problem for the industry,” Shadan said this week at MassDevice.com’s 5th annual DeviceTalks Boston event, “and it’s only going to get worse.” Read more


3. Medtronic’s HeartWare faces 2 Class I FDA recalls

MassDevice.com news

Medtronic said today the FDA labeled 2 outstanding global voluntary recalls related to subsidiary HeartWare International’s HVAD system as Class 1.

A Class 1 indication from the federal watchdog indicates “a reasonable probability that use of these products will cause serious adverse health consequences or death,” according to the agency. Read more


2. Boston Scientific lands $71m Defense Dept. contract

MassDevice.com news

The U.S. Defense Dept. said yesterday that it awarded a contract worth $71 million to Boston Scientific.

The agreement calls for Marlborough, Mass.-based Boston Scientific to provide cardiovascular products to the U.S. Army, Navy, Air Force, Marine Corps and federal civilian agencies. The deal has a 1-year base contract with 4 1-year renewal options, according to the Defense Dept. Read more


1. Report: Terumo eyes Abbott’s cardio biz

MassDevice.com news

Terumo is reportedly eyeing a nearly $1.5 billion deal for Abbott’s cardiovascular device business.

The ¥150 billion deal, if consummated, would be part of Abbott’s move to shed assets and consolidate pending the close of its $25 billion merger with St. Jude Medical, according to Japan’s Nikkei business journal. Earlier this month, Abbott announced plans to deal its medical optics business to Johnson & Johnson for $4.3 billion. Read more

The post MassDevice.com +5 | The top 5 medtech stories for September 30, 2016 appeared first on MassDevice.



from MassDevice http://ift.tt/2djyQBc

Terumo inks regenerative collab deal with Cognate BioServices

Terumo BCT, Cognate BioServicesTerumo Corp. (TYO:4543) and Cognate BioServices said today they inked a collaborative cellular and immunotherapy products development deal.

Get the rest of the story at our sister site, Medical Design & Outsourcing

The post Terumo inks regenerative collab deal with Cognate BioServices appeared first on MassDevice.



from MassDevice http://ift.tt/2ddsGGk

Stereotaxis raises $24m to support

StereotaxisMedical robotics developer Stereotaxis (NSDQ:STXS) said yesterday it closed a $24 million private placement round, floating 24,000 shares of convertible preferred stock and warrants for the purchase of an aggregate 36.9 million shares of common stock.

Each preferred share sold in the round is convertible at the option of the holder at a price of 65¢ per share, St. Louis, Mo.-based Stereotaxis said. The warrants sold have an initial exercise price of 70¢ per share and can be exercised up to 5 years from the closing of the round.

Stereotaxis said it used $13 million raised in the round to “satisfy in full all amounts outstanding under the company’s loan agreement with Healthcare Royalty Partners,” according to an SEC filing.

The investment round was co-led by DAFNA Capital Management and Masimo founder & CEO Joe Kiani, the company said.

In Sept. 2014, Stereotaxis announced FDA clearance for its V-Loop product, the 2nd model from its Vdrive platform to make it to the U.S. market.

The Vdrive with V-Loop technology allows physicians to remotely manipulate a compatible mapping catheter, a device commonly used in the electrophysiology lab. The V-Loop system is compatible with both variable loop and ICE catheters, which are among the most repositioned diagnostic tools during ablation procedures, Stereotaxis said.

The V-Loop system joins V-Sono, another Vdrive product which won FDA clearance in 2013. Stereotaxis’ V-CAS and V-CAS Deflect catheter advancement systems are not yet cleared for the U.S.

The post Stereotaxis raises $24m to support appeared first on MassDevice.



from MassDevice http://ift.tt/2dt3AOh

Mergers, IP, risk assessment among trends in medtech

device-talks-banner-1x1In 1995, the average time to a successful exit for a medical device startup was about 3 years, according to Rotational Medical CEO Martha Shadan. Now, Shadan said, it can range from 6 to 9 years and cost as much as $50 million. Shadan suggested that the increase in exit time is probably due to risk associated with investing in medtech and a lack of venture capitalists.

“This is a real problem for the industry,” Shadan said this week at MassDevice.com’s 5th annual DeviceTalks Boston event, “and it’s only going to get worse.”

Shadan and other medtech executives discussed trends they’re seeing in the industry before a crowd of more than 300 attendees the DeviceTalks event. The panel included Dr. Omar Amirana, a senior VP at Allied Minds; Jeff Mann, senior managing counsel for Med-Surg at Boston Scientific (NYSE:BSX); Christiana Jacxsens, attorney and shareholder at Greenberg Traurig; and Patrick West, a partner at Mirus Capital. David Dykeman, patent attorney and shareholder at Greenberg Traurig, moderated the discussion.

Shadan noted that before Rotation Medical closed a $39 million Series B round in August, she faced a lot of questions about reimbursement from potential investors.

“The number 1 objection and the reason why I heard 47 ‘Nos’ was because of reimbursement risk, and we’re not unusual,” she explained. “This is a huge uncertainty for the med device industry and it’s not getting any better.”

West echoed Shadan’s concerns about the loss of VC funding, adding that mega-mergers between huge companies in the med-tech industry and the lack of R&D funding doesn’t help early-stage companies.

“What you’re seeing is valuations going higher and higher and the options out there for those companies to buy are becoming fewer and fewer. I think we’re in for some interesting times here as we look at going forward,” he said.

The largest 25 acquisitions of 2015 make up about $110 billion in transaction value, but the average transaction value for a company that’s generating revenue is around $150 million. Bigger companies are also moving towards making pre- or early-revenue transactions – acquiring companies that sometimes put up less than $1 million in revenue.

“What’s particularly interesting here is that your average transaction value, as I said, was running around $150 million for the companies with revenue. Of those 22 pre-revenue companies, the average transaction value is over $200 million,” he said.

Amirana said that a company should prepare to be flexible in times of uncertainty.

“In my mind, the number 1 goal of any leader or CEO for a company should be to maintain optionality,” he said. “If the market gets hot, you’re prepared to go public, and you want to do that, you’re capable. If the M&A opportunity presents itself, and that’s what you want to drive to, you should be prepared to do that. If you have to finance the company and drive longer, deeper, further, and build a business that actually generates cash flow, which to many of us might be a dirty word, you need to be prepared to do that.”

Although the panel dedicated much of its time to discussing M&A, they also touched upon the importance of intellectual property and changing patent laws. Amirana said that Allied Minds, a publicly traded private equity group, often looks to license breakthrough technology at universities.

“I see a real strong desire at the university level to commercialize IP, as well as technology,” Dr. Amirana noted. “That is a robust and very active process and activity at the university level.”

Patent laws have changed significantly in the past few years – the U.S. Supreme Court delivered major patent opinions and the American patent system switched to a 1st-to-file protocol, Dykeman noted. He recommended that companies file early and often for incremental improvements, and that they watch their competitors closely.

Shadan added that IP is an important part of strategy and companies should address it as early as possible.

“For instance, if we have technology and we launch in the market for a particular anatomy, but we believe it’s a platform technology, we better be talking about that very, very early, about the potential for a platform,” she explained.

When Mann is doing due diligence for Boston Scientific and investigating an acquisition, he looks at IP as a vital component.

“It’s internalizing what [intellectual property] means, because the freedom to operate and the protection of the portfolio are really the critical pieces,” he said.

Gaps in intellectual property and consumer complaints is often how Jacxsens gets involved with companies, although she would rather work proactively to prevent litigation, she said.

“Coming from my standpoint and background with litigating, it’s a lot more fun and a lot more helpful to help companies on a proactive basis than when you’re dealt with a set of documents or a set of circumstances with that lawsuit in hand,” she said.

“We are well beyond the 1 patient, 1 device malfunction type of litigation here,” she explained. In 1994, she said, there were 70 plaintiffs involved in med-tech cases, compared to 95,000 patients involved in multi-district litigation over product liability today.

A majority of those plaintiffs were involved with the well-known transvaginal mesh lawsuits, which Jacxsens says highlight another problem that companies often overlook when they consider risk.

“You can’t just look at what’s going on with your particular product, but you have to look out there at what’s going on with the product class, what’s going on with that disease state and other devices used to treat that disease or what are other devices that may have the same potential complications,” she said. “It’s thinking broader than just your 1 device and the risks related to your 1 device.”

Despite the concerns about VC funding and difficulties in exiting, the panelists remained optimistic about the future of the industry. “If the technology is breakthrough and it solves an important unmet clinical need, if there is evidence, if there is a strong management team that is executing their plan well, then the money will come in,” Shadan said.

“There are a lot of reasons to believe that this is an exciting space to be in,” West added. “In the end, not only do we hopefully get to make a living doing it, but we’re in an industry where we make a difference in people’s lives, and that’s an unusual opportunity.”

 

The post Mergers, IP, risk assessment among trends in medtech appeared first on MassDevice.



from MassDevice http://ift.tt/2dx5lL4

GE’s venture arm, Allied Minds join forces

GE Ventures, Allied MindsGE Healthcare‘s (NYSE:GE) Venture arm said today it signed a strategic alliance with Boston-based innovation development group Allied Minds to develop and commercialize “next-generation technologies.”

Through the deal, GE and Allied Minds will invest in both new and existing tech sourced from both company’s pipelines, both existing and new. Allied Minds will recive exclusive right of first refusal to license tech, chosen by GE, which are “of strategic interest” to the companies. GE will also gain the opportunity to invest in Allied Minds innovations.

“What drives Allied Minds is disruption of the status quo in cooperation with our research partners. Our new partnership with GE, a globally-renowned leader in innovation, allows us to begin tapping into the vast potential of IP being developed within the laboratories of leading commercial companies. Allied Minds is delighted to work with GE and to gain direct access to its technologies while providing GE with exposure to Allied Minds’ portfolio and pipeline of innovations sourced from its network of partners,” Allied Minds CEO Chris Silva said in a press release.

Allied Minds reviews intellectual opportunities from universities and federal labs, seeking to identify potentially commercially impactful innovations, and funding, managing and building subsidiary companies to support tech that passes due diligence.

“GE is excited to have Allied Minds as a channel partner for venture creation. Allied Minds’ capabilities and experience in early stage technology development complement GE’s diverse IP portfolio. We look forward to building opportunities with our combined expertise,” GE Ventures licensing prez Pat Patnode said in prepared remarks.

The post GE’s venture arm, Allied Minds join forces appeared first on MassDevice.



from MassDevice http://ift.tt/2cQSbKz

Medtronic’s HeartWare faces 2 Class I FDA recalls

Medtronic pays $1B for HeartWareMedtronic (NYSE:MDT) said today the FDA labeled 2 outstanding global voluntary recalls related to subsidiary HeartWare International‘s HVAD system as Class 1.

A Class 1 indication from the federal watchdog indicates “a reasonable probability that use of these products will cause serious adverse health consequences or death,” according to the agency.

The voluntary recall is related to potential damage to controllers on the device from exposure to moisture, caused by loose power and data connectors, according to a Medtronic press release. The company added that, in the U.S., all clinicians have been notified and acknowledged, while 99% of clinician notifications have been acknowledged globally.

In a warning sent in May and June, HeartWare advised hospital clinicians to inspect HVAD HeartWare controllers for loose connectors during scheduled appointments, and to replace affected controllers with new equipment when necessary. Clinicians were also instructed to communicate safe use instructions for the HVAD system, with a focus on moisture and proper connection to power and data sources.

Damage to the controllers from the stated issue can potentially cause a loss of communication between the controller and the monitor, with reduced ability to detect alarms or interruptions of support due to a pump stop. These issues could result in serious injury or death, Medtronic warned.

The recall affects approximately 8,799 units with model numbers 1400 and 1401, distributed worldwide. A total 308 controller units have been replaced as of Sept. 26, the company said.

A separate global voluntary recall, initiated in August, affected un-implanted, sterile HVAD pump implant kits in hospital inventory. The pumps supplied in the kits could be susceptible to electrical faults and connection failures if fluid enters the driveline-to-controller connector during or after the implant procedure, Medtronic said.

The issue could result in serious injury or death due to electrical faults or connection failures interrupting circulatory support, the company said. Eighty-nine percent of patients globally have acknowledged notifications for the issue, Medtronic added.

The 2nd recall affects model numbers 1103 and 1104 with serial numbers lower than HW25838. As of today, 350 potentially affected kits have been distributed worldwide, with 323 having been returned to HeartWare already.

Medtronic closed its $1.1 billion acquisition of HeartWare in late August.

The $58-per-share deal cleared the field of the 2 major cardiac assist device makers, after Medtronic’s cross-town rival, St. Jude Medical (NYSE:STJ), paid $3 billion for Thoratec in October 2015 (St. Jude is now being acquired by Abbott (NYSE:ABT) for $25 billion). HeartWare’s implantable left ventricular assist devices are designed for end-stage heart failure patients, either as a destination therapy until death or as a bridge to heart transplantation.

The post Medtronic’s HeartWare faces 2 Class I FDA recalls appeared first on MassDevice.



from MassDevice http://ift.tt/2dsFqne

Boston Scientific lands $71m Defense Dept. contract

Boston ScientificThe U.S. Defense Dept. said yesterday that it awarded a contract worth $71 million to Boston Scientific (NYSE:BSX).

The agreement calls for Marlborough, Mass.-based Boston Scientific to provide cardiovascular products to the U.S. Army, Navy, Air Force, Marine Corps and federal civilian agencies. The deal has a 1-year base contract with 4 1-year renewal options, according to the Defense Dept.

Earlier this week, Boston Scientific agreed to pay $210 million for EndoChoice (NYSE:GI) and its line of devices for treating gastrointestinal disease.

The $8-per-share offer is slated to close by the end of the year, the companies said. EndoChoice took itself public in June 2015 with an IPO that brought in some $96 million.

The post Boston Scientific lands $71m Defense Dept. contract appeared first on MassDevice.



from MassDevice http://ift.tt/2dshxMu

Report: Terumo eyes Abbott’s cardio biz

Terumo, AbbottTerumo (TYO:4543) is reportedly eyeing a nearly $1.5 billion deal for Abbott‘s (NYSE:ABT) cardiovascular device business.

The ¥150 billion deal, if consummated, would be part of Abbott’s move to shed assets and consolidate pending the close of its $25 billion merger with St. Jude Medical (NYSE:STJ), according to Japan’s Nikkei business journal. Earlier this month, Abbott announced plans to deal its medical optics business to Johnson & Johnson (NYSE:JNJ) for $4.3 billion.

Terumo is interested in other, unspecified assets owned by Abbott, according to the report.

For its part, Terumo is expanding its footprint in medical devices. The Japanese company put up to $380 million on the table in July for Sequent Medical and its Web aneurysm embolization device. Terumo paid $2.62 billion for CaridianBCT in 2011.

 

The post Report: Terumo eyes Abbott’s cardio biz appeared first on MassDevice.



from MassDevice http://ift.tt/2dgm720

Using symbols to convey information in medical device labeling

FDA VoiceBy: Antoinette (Tosia) Hazlett, MSN, RN, and Scott Colburn CAPT, USPHS

Symbols convey important messages for navigating everyday life; whether it’s a traffic sign or a graphic image indicating that no smoking is allowed in a building. Symbols in medical device labeling can also convey important information. However, to be an effective means of communicating information, it’s critical that symbols on medical devices are understood by the individuals who use them.

In June, FDA issued the Use of Symbols in Labeling final rule, which describes the circumstances in which manufacturers can use a stand-alone symbol in device labeling without any adjacent explanatory text. For example, if certain requirements are met under the final rule, manufacturers of sterile syringes could opt to use the symbol for “do not reuse” on a syringe package without adding the actual words “do not reuse” to the package.

Using Symbols

The “Use of Symbols in Labeling” final rule which went into effect on September 13, 2016, does not mandate the use of stand-alone symbols in device labeling. Under the final rule, device manufacturers have three options. They can choose not to use symbols, use symbols with adjacent explanatory text, or use stand-alone symbols that have been established in a standard if certain requirements are met, including providing an explanation of the symbols in a symbols glossary that is included in the labeling for the device.

Adding the option of stand-alone symbols is expected to reduce design costs for manufacturers because it is more consistent with how devices are currently labeled in Europe and other foreign markets. Replacing small and difficult-to-read text with a symbol will also help make some labeling more user-friendly and understandable. That is critical in medical device labeling, where space may be limited. The use of stand-alone symbols on a global scale may help promote better understanding through consistent labeling across products distributed in the U.S. and foreign markets.

Before this rule, FDA recognized five consensus standards that address the use of stand-alone symbols. On the same day this rule was issued, FDA updated its currently recognized consensus standards list and added three new standards containing more symbols in a published standards-recognition notice.

Symbols Glossary

The required symbols glossary is intended to help users become familiar with the meaning of the stand-alone symbols and serve as a reference for users to look up any definitions they may not recall.

The symbols glossary may be in a paper or electronic format as long as it is included in the labeling for the device. Additionally, the labeling on or within the package that contains the device must bear a prominent and conspicuous written statement identifying the location of the symbols glossary.

Symbol Statement “Rx Only” or only”

The rule also allows for the use of the commonly used symbol statement “Rx only” or “℞ only” in the labeling for prescription devices.

Learn More

On Monday, July 25, 2016, FDA conducted a webinar to help industry and patient groups learn more about this final rule and the new standards recognition notice. The slides, recording and transcript from the webinar entitled, “Final Rule: Use of Symbols in Labeling” is available on the CDRH Learn  and Webinar webpages.

fda-voice-hazlett-1x1Antoinette (Tosia) Hazlett, MSN, RN, is a Senior Policy Analyst at FDA’s Center for Devices and Radiological Health

 

 

fda-voice-colburn-1x1Scott Colburn CAPT, USPHS, is FDA’s Director, Center for Devices and Radiological Health Standards Program

 

 

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

The post Using symbols to convey information in medical device labeling appeared first on MassDevice.



from MassDevice http://ift.tt/2dABIfZ

dijous, 29 de setembre del 2016

InspireMD pulls trigger on 1-for-25 reverse split

InspireMDInspireMD (NYSE:NSPR) said yesterday it initiated a 1-for-25 reverse split of its stock, effective Oct. 7, with its stock trading on a split adjusted basis starting Oct. 10.

The move will reduce the shares of InspireMD on the market by putting 1 share of common stock in the hands of shareholders for every 25 shares they held previously. No fractional shares will be distributed in the reverse split, the company said.

The reverse split was approved at a special meeting of stockholders held yesterday, Boston-based InspireMD said.

The number of authorized shares of the company’s common stock will remain at 150 million, while the number of outstanding shares will be reduced from approximately 36 million to 1.4 million, according to a press release.

In July, InspireMD said it raised $14.6 million in a “best efforts” stock offering it plans to use to boost sales of its anti-stroke devices.

InspireMD said the offering consisted of 442,424 shares of Series B stock convertible into 100 shares of common stock at 33¢ per share, with a 5-year cumulative dividend rate of 15% a year. The offering also included warrants for more than 44.2 million shares of common stock at an exercise price of 20¢ per share, the company said.

The post InspireMD pulls trigger on 1-for-25 reverse split appeared first on MassDevice.



from MassDevice http://ift.tt/2cZzwKr

Sunshine Heart shifts focus to Aquadex FlexFlow system

Sunshine Heart shifts focus to Aquadex FlexFlow systemSunshine Heart (NSDQ:SSH) said today it will realign its strategy to focus on its recently acquired Aquadex FlexFlow system, designed to filter water and salt from patients with fluid overload due to renal failure.

The Eden Prairie, Minn.-based company acquired the system from Baxter for $5 million in August this year. It also said it will pause clinical evaluations of its neuromodulation tech and reduce cash burn to $80,000 per month in the 4th quarter of 2016.

The company is targeting $5 million in annual revenue for the Aquadex business in the 4th quarter of 2016, and $10 million in  the 4th quarter of 2017, Sunshine Heart reported.

The company’s flagship product is C-pulse, a counterpulsation device that is designed to reduce the load on the left ventricle with a cuff around the aorta that beats in sync with the heart’s pulsation.

The strategy realignment for Sunshine Heart comes after it said in July it would shift from counterpulsation to neuromodulation tech.

“Aquadex was an important strategic investment, which allows Sunshine Heart to strengthen its presence in the heart failure market,” chairman & CEO John Erb said in prepared remarks. “We have been very pleased with the reception and enthusiasm we have received from many current and former Aquadex customers that depend on Aquapheresis Therapy to manage fluid overload, including patients with congestive heart failure. Aquadex has shown to help reduce the length of stay while in the hospital and the number of unscheduled hospital visits in total.”

SSH shares dropped to $0.60 apiece, down 14%, in mid-afternoon trading activity.

The post Sunshine Heart shifts focus to Aquadex FlexFlow system appeared first on MassDevice.



from MassDevice http://ift.tt/2cOVXEw

iBeat launches wearable heart monitor

iBeat launches wearable heart monitoriBeat said today that it launched its wearable heart monitor on Indiegogo. The campaign began this morning and features a 78% sale on the device at $99 for 100 early-bird backers.

The San Francisco, Calif.-based start-up raised $1.5 million in seed funding in August to recruit “high profile talent” to expand its operations. Dr. Mehmet Oz joined the company as a special advisor and is assisting in the launch, according to iBeat.

The iBeat Life Monitor is a smartwatch that continuously monitors a user’s heart rate and will warn loved ones and emergency responders if it detects signs of an oncoming cardiac arrest and the user is unresponsive.

It’s equipped with GPS to provide a user’s location to first responders in case of an emergency. The wearable monitor is cellular, so it doesn’t require WiFi or Bluetooth connectivity to function.

“The early interest we’ve seen in iBeat has been remarkable,” founder and CEO Ryan Howard said in prepared remarks. “We are excited to bring our device to the Indiegogo platform to drive even more awareness around the product and its ability to potentially save someone’s life. If you suffer a life-threatening heart incident such as sudden cardiac arrest, you have a 90% chance of dying without intervention. There are many devices on the market including diabetic monitors, heart-rate monitors, and other health monitoring solutions, but all these devices only passively monitor you. None of them actively monitor and analyze your heart health around-the-clock like the iBeat Life Monitor. Continual monitoring and quick intervention can mean the difference between life and death in emergency situations.”

The post iBeat launches wearable heart monitor appeared first on MassDevice.



from MassDevice http://ift.tt/2dq8go2

Taking the risk out of manufacturing transfers: Four best practices

vention-october2016-350If you’re considering a manufacturing transfer, you may be losing sleep over all the things that could go wrong:

  • cost overruns
  • schedule slips
  • quality issues, to name a few.

Missteps anywhere in the process can make the difference between meeting or missing your timeline and budget.

vention-logo

The post Taking the risk out of manufacturing transfers: Four best practices appeared first on MassDevice.



from MassDevice http://ift.tt/2dezTlB

Tackling the gender disparity in medtech

device-talks-banner-1x1Over the course of her 30 year career in medtech, IBM Watson Health general manager Deborah DiSanzo has been a firsthand witness to the effects of gender imbalance within the industry. She started as a project manager for Apollo Computer, and after Apollo was bought by Hewlett-Packard, DiSanzo recalled there were plenty of women working beside her. “I can now point to 1 woman who’s still in medtech from that,” DiSanzo said.

Deborah DiSanza

Deborah DiSanzo

A panel of female medtech executives discussed the under-representation of women in the medical device industry to a crowd of over 300 people at MassDevice’s 5th annual DeviceTalks this week. The panel included  DiSanzo,  InfoBionic CEO Nancy Briefs, and Rotation Medical CEO Martha Shadan. Brad Perriello, executive editor and co-founder of MassDevice, moderated the panel.

Data published in a survey conducted by LeanIn.org and McKinsey & Co. show a clear pattern – women hold 45% of entry level positions, but only 19% of C-suite roles. Just 5% of Fortune 400 CEOs are women. The study reported that for every 100 women promoted to a managerial role, 130 men are promoted.

Briefs recalled that when she was first recruited by a leading heart valve company in the early stage of her career, they told her that part of the reason she was hired was to fill an employment quota.

“I went on to become the rookie of the year, and all of the men in my group were so supportive,” she said. “I have to say that I got off to a really great start. I was the only woman in the sales force at the time of I think about 80 to 100 people.”

All of the women noted that when they gathered for corporate events with their predominately-male colleagues, the activities were always geared toward men.  Shadan explained that one company event, the choices were paintballing or mountain biking. Briefs chimed in, adding that she and her colleagues were once offered a choice between golf, cigars, or running a half marathon.

Martha Shadan

Martha Shadan

With DiSanzo and Shadan at the helm of their companies, both IBM Watson Health and Rotation Medical have gotten closer to achieving equal gender representation. Shadan reported that 40% of Rotation Medical’s employees are women and that there are 3 in the C-suite. Watson Health’s executive team is 40% women, according to DiSanzo.

Despite slow progress towards gender equality, attitudinal biases against women in leadership roles still exist, Shadan acknowledged.

“I learned very early in my career that I had to subjugate having feelings or displaying feelings in the workplace,” she explained. “So, it has been difficult as a woman, especially moving up in the ranks, to be true to myself, who I am, to display authentic leadership, yet be able to fit in.”

As women become equal contributors to the medtech industry, companies are focusing on how to achieve equal compensation. Briefs said that for start-ups, it’s as simple as ensuring that compensation equity is an early part of their strategy. If you want to attract the strongest talent, Briefs said, a solid compensation plan is critical.

DiSanzo added that equal compensation often comes when companies and industries make that information available to the public. “Transparency is key,” she said. “When you look at it, you can change it.”

Briefs, DiSanzo, and Shadan agreed that it’s not just about ensuring gender equality in the industry – it’s about diversity in general. “It is important to have more women but I think fundamentally it’s important to have divergence of thought,” Shadan explained.

“If you just look at the statistics it says the more inclusive, the better their performance,” Briefs noted. “I think performance at the end of the day in the business is what we’re all driving for.”

Looking ahead, these 3 executives expressed excitement about the industry and for the innovation that diversity can bring to medtech. “I certainly hope that the woman who’s standing here 30 years from now doesn’t have to say that of the women I started with, there’s only 1 that I know today,” DiSanzo said.

The post Tackling the gender disparity in medtech appeared first on MassDevice.



from MassDevice http://ift.tt/2cOSHZC

Avita inks Iranian distro deal

Avita MedicalAvita Medical (ASX:AVH) said today it will be entering the Iranian market after inking a distribution deal with Iran-based Teb Sanaat Lotus and its Iranian partner company Zikad International Aesthetics Supplier.

As part of the deal, a dedicated clinic using Avita’s regenerative medical devices will open in Tehran, the company said.

“Using our strong distribution network and distinguished medical contacts, we are confident that we can create a strong demand for Avita’s ReNovaCell and its other regenerative skin healing products in Iran. There is real excitement about this unique approach and how we can deploy it to give better outcomes in these sizable patient groups” Zikad Int’l Aesthetics Supplier’s Aram Mousavi said in a press release.

The initial focus of the center will be on aesthetics, including repigmentation and scar reconstruction. The company said Zikad plans to expand into treatments for burns and chronic wounds in the coming months.

“Using a dedicated clinic is a new approach for Avita, and we believe it will give us real focus to reach this important market. The dedicated ReNovaCell clinic and training center should support the rapid adoption of our skin renewal technology. And when this platform is further rolled out to burns and chronic wounds, we anticipate Iran will become a significant market for Avita,” CEO Adam Kelliher said in prepared remarks.

Avita said its ReCell device was a good fit for the region, which records approximately 150,000 burn sufferers every year – numbers 8 times higher than the average global rate. The company said it will provide clinical support to Zikad’s sales team and extended agent network.

In July, Avita said it raised $9 million in a partially underwritten rights issue for its ReCell device, which is designed to use a patient’s own skin cells to treat burns, chronic wounds and skin defects.

Avita, which has offices in Northridge, Calif., Cambridge, U.K. and Perth, Australia, said it issued nearly 100.2 million new shares in the offering, which closed July 4.

The company said July 10 that it plans to use the funds in part to ramp up its U.S. commercial operations ahead of an expected approval, and on “building commercial traction” in China and Australia, where it’s already on the market.

The post Avita inks Iranian distro deal appeared first on MassDevice.



from MassDevice http://ift.tt/2daW404

The 6 Sciences of Medical Micro Molding

mtd-october2016-300The medical micro molding industry is still fairly young, but is rapidly growing and evolving. Being aware of shifts in trends and changes in technology helps to see where ­and how­ the next major innovations and breakthroughs will occur. In the medical device world, it’s often the smallest parts that carry the greatest importance relative to the functionality and safety of a medical device. More than ever, embracing the best proven processes and tools for manufacturing is critical to successful product development.

This whitepaper explores:

  • Market and industry trends
  • Industry challenges
  • The 6 Sciences of Micromolding
  • Steps to successful R&D and product launch

By implementing these six sciences, medical OEMs will understand how to maximize the tools needed for efficient product development and consistent manufacturability in micro molding -­ and to create product breakthroughs today.

mtd-logo

The post The 6 Sciences of Medical Micro Molding appeared first on MassDevice.



from MassDevice http://ift.tt/2ddppV7

5 Steps to Medical Device Commercialization in the U.S.

intertek-whitepaper-september2016-smallSpeed your medical devices to market with this complimentary guide which takes you step by step through the process of submitting your medical devices for approval from the FDA.
As a leader in third party testing and certification, our industry experts developed this guide to simplify the complex process to submit your medical devices to the FDA and provide an in-depth understanding of all that is involved, including:

  • Classifying your device
  • Identifying the correct premarket submission
  • Preparing the premarket submission
  • Submitting to the FDA
  • Establishing a registration and device listing

download-now-button

The post 5 Steps to Medical Device Commercialization in the U.S. appeared first on MassDevice.



from MassDevice http://ift.tt/2dDbnKA

Medtronic issues urgent field safety notice for select ICDs, CRTds

MedtronicMedtronic (NYSE:MDT) issued an urgent field safety notice concerning issues with specific units of its Viva cardiac resynchronization therapy defibrillators and Evera implantable cardioverter defibrillators that could result in rapid battery depletion.

The Fridley, Minn.-based company sent the notice on August 12 to healthcare professionals managing patients with the devices. The notice warned of issues with 78 specific Viva CTR-D and Evera ICDs related to a specific subset of circuit components which may have a low resistance path that could result in rapid battery depletion.

Medtronic said that, based on its records, 53 of the 78 devices are still active.

The low resistance path in the circuit can result in depletion of the battery in 7 days or less, Medtronic said, warning health care providers that the issue may present itself in follow up visits.

The company said the issue could manifest in 1 or more electrical resets, lack of pacing or defibrillation therapy output, no telemetry or a programmer screen display of “SERIOUS DEVICE MEMORY FAILURE.” Medtronic warned that audible alerts and CareAlerts may not reliably notify the patient or clinician due to the issue.

A total of 7 confirmed failures have been reported since July 16, Medtronic said. The company said it expects an additional 6 failures, as predicted by modeling, in the remaining active population.

Reported complications include shortness of breath, pocket heating, low heart rate and early device explant. No deaths have been reported related to the issue.

The company instructed managing clinicians to advise patients to seek medical attention immediately if they experience any symptoms or if they experience audible patient alerts. Further, more detailed instructions were included for patients with whom explant is not the best course of action.

Medtronic said it notified the appropriate authorities of the failure.

The post Medtronic issues urgent field safety notice for select ICDs, CRTds appeared first on MassDevice.



from MassDevice http://ift.tt/2cEW9D2

MassDevice.com +5 | The top 5 medtech stories for September 29, 2016

plus5-node

Say hello to MassDevice +5, a bite-sized view of the top five medtech stories of the day. This feature of MassDevice.com’s coverage highlights our 5 biggest and most influential stories from the day’s news to make sure you’re up to date on the headlines that continue to shape the medical device industry.

Get this in your inbox everyday by subscribing to our newsletters.

 

5. Si-Bone wins Nebraska BCBS coverage for iFuse implant system

MassDevice.com news

Si-Bone said today Blue Cross Blue Shield of Nebraska updated its medical policy to provide coverage for minimally invasive SI joint fusion procedures.

The move makes BCBS of Nebraska the 2nd BCBS plan, following BCBS of Michigan, to approve a positive coverage policy for MIS SI joint fusion procedures, San Jose, Calif.-based Si-Bone said. Read more


4. DePuy Synthes recalls select medical power tool battery packs over explosion risk

MassDevice.com news

Johnson & Johnson subsidiary DePuy Synthes initiated a select recall of power tool system battery adaptors due to possible explosion risks, according to an FDA notice posted today.

The federal watchdog labeled the recall as a Class I, the most serious type of recall issued, indicating “a reasonable probability that use of these products will cause serious adverse health consequences or death.” Read more


3. Edwards Lifesciences wins CE Mark for Inspiris Resilia aortic valve

MassDevice.com news

Edwards Lifesciences said today it won CE Mark approval in the European Union for its Inspiris Resilia aortic valve.

The Irvine, Calif.-based company said the valve is the 1st in a “new class of resilient heart valves” which incorporate its Resilia tissue and features a Perimount Magna ease valve and VFit technology for future valve-in-valve procedures. Read more


2. Misonix reports Chinese distributor to SEC, DOJ over possible FCPA issues

MassDevice.com news

Misonix this week reached out to the Securities and Exchange Commission and the U.S. Department of Justice over possible issues with the Chinese distributor of its products, according to an SEC filing posted today.

The company said that on Sept. 27 and Sept. 28, respectively, it contacted the SEC and DOJ to “voluntarily inform” them that it may have “had knowledge of certain business practices of the independent Chinese entity that distributes its products in China, which practices raise questions under the Foreign Corrupt Practices Act. Read more


1. Intuitive Surgical inks R&D JV deal with Fosun Pharma for catheter-based robotic systems

MassDevice.com news

Robotic surgery giant Intuitive Surgical said today it inked a joint venture deal with Shanghai Fosun Pharmaceutical to research, develop, manufacture and sell robotic-assisted catheter-based medical devices.

Both companies will contribute $100 million to start the joint venture, which will initially focus on development of early diagnostics and cost-effective treatments for lung cancer, one of the most commonly diagnosed forms of cancer in the world. Read more

The post MassDevice.com +5 | The top 5 medtech stories for September 29, 2016 appeared first on MassDevice.



from MassDevice http://ift.tt/2do3VoV

Becton Dickinson invests $40m in Irish plant expansion

Becton DickinsonBecton Dickinson & Co. (NYSE:BDX) said this week it is investing $40.4 million (EU €36 million) to expand production equipment at its Drogheda, Ireland facility, adding an additional 20 jobs.

The Franklin Lakes, N.J.-based company’s Drogheda facility produces BD PosiFlush syringes and safety components designed for insulin injection. The $40.4 million investment will allow for 2 new production lines at the plant, with the 1st manufacturing line having already commenced production.

“Today’s announcement that Becton Dickinson is to create an additional 20 jobs and invest €36m at their Drogheda plant is a significant boost for the local economy of the North East region. This investment demonstrates the company’s long term commitment to Ireland and builds on its 50-year history in Drogheda,” IDA Ireland CEO Martin Shanahan said, according to a report from BusinessWorld.

The addition of new jobs will boost the total workforce at the facility up to 150, according to the report.

The investment is the 3rd into its production facilities in the last month. Last week, BD announced a $100 million investment to expand its Holdrege, Neb.-based facility to make extra room for insulin syringe manufacturing operations.

The investment will support new manufacturing equipment and tech to expand production for BD insulin syringes, the company said. The companycurrently produces more than 2 billion insulin syringes per year.

In August, BD said it was investing $20 million to upgrade its Sandy, Utah facilities which make IV catheters and valves, blood collection devices and surgical products.

BD said the site dates back to Deseret Pharmaceutical, which opened in Murray, Utah, in 1956. The company bought the plant in in 1986 and grew it to 550,000 square feet and 1,200 employees.

The post Becton Dickinson invests $40m in Irish plant expansion appeared first on MassDevice.



from MassDevice http://ift.tt/2dhnTA5

Misonix reports Chinese distributor to SEC, DOJ over possible FCPA issues

MisonixMisonix (NSDQ:MSON) this week reached out to the Securities and Exchange Commission and the U.S. Department of Justice over possible issues with the Chinese distributor of its products, according to an SEC filing posted today.

The company said that on Sept. 27 and Sept. 28, respectively, it contacted the SEC and DOJ to “voluntarily inform” them that it may have “had knowledge of certain business practices of the independent Chinese entity that distributes its products in China, which practices raise questions under the Foreign Corrupt Practices Act.

The company said its audit committee and board of directors have engaged outside counsel to conduct an internal investigation to review those, and other, matters, and that the investigation is ongoing.

Currently, Misonix said it has no information from the investigation or otherwise that would suggest its previously reported financial statements and results are “incorrect in any material respect,” according to an SEC filing.

“The company intends to cooperate fully with the DOJ and SEC as the investigation continues. At this stage, the company is unable to predict what, if any, action the DOJ or the SEC may take or what, if any, penalties or remedial measures these agencies may seek,” Misonix wrote in an SEC filing.

Misonix said that any ruling that found the company’s operations or activities are outside compliance with laws or regulations could mean fines, civil and criminal penalties.

The filing follows the announcement that Misonix would delay its annual report due to “deficiencies” in its internal financial reporting controls, which it declared earlier this month.

The Farmingdale, N.Y.-based company also said it named Joseph Dwyer as interim CFO, replacing Richard Zaremba, who was named senior finance VP.

The post Misonix reports Chinese distributor to SEC, DOJ over possible FCPA issues appeared first on MassDevice.



from MassDevice http://ift.tt/2cZ24n8

DePuy Synthes recalls select medical power tool battery packs over explosion risk

DePuy Synthes logoJohnson & Johnson (NYSE:JNJ) subsidiary DePuy Synthes initiated a select recall of power tool system battery adaptors due to possible explosion risks, according to an FDA notice posted today.

The federal watchdog labeled the recall as a Class I, the most serious type of recall issued, indicating “a reasonable probability that use of these products will cause serious adverse health consequences or death.”

The company said they are recalling the Adaptor and Light Adaptor for their SBD and SBD II due to a potential for the adaptors “to produce extreme internal pressure, which may cause the device to explode.” Such a failure could cause serious adverse health consequences, including death.

The recall affects a total of 451 units, according to the release. Serial numbers 05.001.024 and 05.001.108 were identified in the recall, with manufacturing dates between Oct. 6, 2005 and April 5, 2016 and distribution dates between Jan. 2006 and June 2016.

DePuy Synthes said it sent a letter to affected customers in January, instructing them to identify and quarantine affected devices and contact the company to continue the process of returning and replacing the units.

The post DePuy Synthes recalls select medical power tool battery packs over explosion risk appeared first on MassDevice.



from MassDevice http://ift.tt/2dCP87N

Israel’s Sino-Lite picks up dental laser maker Light Instruments

Light InstrumentsIsraeli medical and dental group Sino-Lite said today it acquired formerly Syneron Medical Ltd.-owned (NSDQ:ELOS) dental laser maker Light Instruments for an undisclosed amount.

Light Instruments develops and produces dental laser technology for hard and soft tissue treatments, including its flagship LiteTouch laser-in-handpiece non-fibre Er:YAG dental laser device, Sino-Lite said.

“The acquisition of Light Instruments is the first step within a sequence of acquisitions of high technology companies and innovative companies that the group intends to acquire in the Israeli market. The new leadership will drive the LiteTouch technology brand forward and further develop its valued innovative contribution to the dentistry world. Sino-Lite Ltd. shall increase Light Instruments workforce and expand the variety of high-end advanced technology dental lasers offered, thus affirming its position as a worldwide global leader,” Sino-Lite CEO Eric Ben-Mayor, who will now serve as CEO of Light Instruments, said in a prepared statement.

Sino-Lite said it specializes in acquisitions, development and management of dental and medical companies and is backed by Chinese groups, including Sino-Ita International Trading Company.

The company touted the purchase, saying the dental laser market “is 1 of the biggest potential markets in the coming decade.”

The post Israel’s Sino-Lite picks up dental laser maker Light Instruments appeared first on MassDevice.



from MassDevice http://ift.tt/2d8Q2K6

Intuitive Surgical inks R&D JV deal with Fosun Pharma for catheter-based robotic systems

Intuitive Surgical, Fosun PharmaceuticalsRobotic surgery giant Intuitive Surgical (NSDQ:ISRG) said today it inked a joint venture deal with Shanghai Fosun Pharmaceutical (SHA:600196) to research, develop, manufacture and sell robotic-assisted catheter-based medical devices.

Both companies will contribute $100 million to start the joint venture, which will initially focus on development of early diagnostics and cost-effective treatments for lung cancer, one of the most commonly diagnosed forms of cancer in the world.

“We are excited to deepen our partnership with Fosun Pharma focused on delivering innovative healthcare solutions in China and around the world. We are proud to make this important long-term commitment to China,” Intuitive Surgical CEO Dr. Gary Guthart said in a press release.

Technologies developed through the JV will be used in catheter-based robotic-assisted medical devices and will include incorporated proprietary intellectual property developed or owned by Intuitive Surgical, the companies said.

The JV will be registered in Shanghai, where all R&D and manufacturing will take place. Distribution inside China will be conducted by the JV, while distribution outside the region will be carried out by Intuitive Surgical, the Sunnyvale, Calif.-based company said.

“We are pleased to expand our partnership and advance the development of medical tools to enhance the wellbeing of global populations, including those in China that suffer from increased rates of lung cancer. The cooperation will boost the development of Fosun Pharma’s medical device sector by integrating branding concept, matching resources and leveraging complementary advantages with Intuitive Surgical, so as to bring better medical tools for doctors,” Fosun Pharma chairman Chen Qiyu said in a prepared statement.

Fosun Pharma subsidiary Chindex Medical Limited has operated as a distribution partner for Intuitive’s da Vinci systems in China since 2011.

Last month, Intuitive Surgical released data from a study of its da Vinci robotic surgical system used during ventral hernia procedures, touting low rates of conversion, intra-operative complications and 30-day post-operative complications.

Data from the study was recently published in the journal Surgical Endoscopy, Intuitive Surgical said.

The post Intuitive Surgical inks R&D JV deal with Fosun Pharma for catheter-based robotic systems appeared first on MassDevice.



from MassDevice http://ift.tt/2dulO7r

Becton Dickinson wins 510(k) for Vacutainer Barricor tubes

Becton DickinsonBecton Dickinson & Co. (NYSE:BDX) said today it won FDA 510(k) clearance for its Vacutainer Barricor plasma blood collection tube.

The Franklin Lakes, N.J.-based company touted improvements to the next-gen blood collection and separation device, saying its designed to improve sample quality, speed up result returns and improve patient care and clinical efficiency.

“As we launch BD Barricor tubes in the U.S., we are effectively eliminating the tradeoff of superior sample quality versus quick turnaround often faced by laboratory technicians by providing both a cleaner and faster plasma sample than current methods. This revolutionary technological advancement can improve the accuracy and speed of clinical decision making, and result in enhanced patient care,” preanalytical systems worldwide prez John Ledek said in a prepared statement.

The BD Barricor tube is a single-use, plastic, evacuated tube obtain plasma for in vitro diagnostic use, and operates with a novel mechanical separation technology to obtain plasma from whole blad samples. The company said the mechanical separator technology is designed to reduce centrifugation time from 10 minutes to 3 minutes and reduce cellular contamination by 50 to 65% compared to plasma gel tubes.

The company said the device is now commercially available in the U.S.

Last week, Becton Dickinson said it is investing $100 into expanding its Holdrege, Neb.-based facility to make extra room for insulin syringe manufacturing operations.

The investment will support new manufacturing equipment and tech to expand production for BD insulin syringes, the company said. BD currently produces more than 2 billion insulin syringes per year.

The post Becton Dickinson wins 510(k) for Vacutainer Barricor tubes appeared first on MassDevice.



from MassDevice http://ift.tt/2cO57ky

Edwards Lifesciences wins CE Mark for Inspiris Resilia aortic valve

Edwards Lifesciences' Inspiris ResiliaEdwards Lifesciences (NYSE:EW) said today it won CE Mark approval in the European Union for its Inspiris Resilia aortic valve.

The Irvine, Calif.-based company said the valve is the 1st in a “new class of resilient heart valves” which incorporate its Resilia tissue and features a Perimount Magna ease valve and VFit technology for future valve-in-valve procedures.

“The Inspiris valve creates a new class of surgical valves and includes key patient-focused innovations, such as the resilient tissue and the VFit technology, to advance the treatment of patients with heart valve disease. In partnership with surgeons, Edwards is committed to developing differentiating technologies that set a new standard for surgical heart valves,” surgical heart valve therapy corp veep Bernard Zovighian said in a press release.

The company touted its Resilia tissue as a 1st-of-its-kind tissue platform designed with improved anti-calcification properties and sustained hemodynamic performance.

European approval of the valve was obtained with support from the company’s Commence pivotal trial, Edwards said, which reported no cases of structural valve deterioration, valve thromboses or nonstructural valve dysfunction at 1-year. Data from separate pre-clinical studies indicated significantly reduced calcification and sustained hemodynamics compared with current treatment options, Edwards said.

“Heart valve patients are living longer and want to maintain their active lifestyles. The Inspiris valve provides surgeons and their patients with an advanced treatment option that represents an ideal foundation for the future treatment of heart valve patients,” Dr. Vinayak Bapat of London’s Guy’s and St. Thomas’ Hospital said in prepared remarks.

Edwards said it is planning a targeted commercial release of the valve in Europe in the 4th quarter of this year, with a full launch in the 1st quarter of 2017.

Earlier this month, Edwards Lifesciences said it won CE Mark approval in the European Union for an expanded indication for its Sapien 3 transcatheter aortic valve replacement.

The expanded indication covers patients at intermediate risk for open heart surgery, Irvine, Calif.-based Edwards said. Last month the FDA also expanded the Sapien 3 indication to include intermediate-risk aortic stenosis patients. The device won its original CE Mark approval back in January 2014, with the U.S. federal safety watchdog following suit in June 2015.

The post Edwards Lifesciences wins CE Mark for Inspiris Resilia aortic valve appeared first on MassDevice.



from MassDevice http://ift.tt/2dxhIel

DeviceTalks Podcast: Talking culture with Smiths Medical CEO Jeffery McCaulley

Jeffery McCaulley came to Smiths Medical with the job of turning a flagging medical device franchise around after years of negative growth. Getting rid of the wood paneling was another story.

McCaulley, a 25-year veteran of the medical device business, held executive level positions at Zimmer Holdings and Medtronic. However, there was nothing that taught him more about culture than his time at GE Healthcare. Like so many of his colleagues in the industry, McCaulley started his career at the now Boston, Mass.-based corporate juggernaut, and serving under now GE CEO Jeff Immelt.

In this interview, we sat down with McCaulley to talk about corporate culture, why he thinks it’s so important, what he did to change the culture at Smiths Medical and his down-to-the-studs rebuild of the company’s Minnesota headquarters, where he replaced the wood paneled executive offices of the past with a new, open flow, design that is built to foster innovation.

The post DeviceTalks Podcast: Talking culture with Smiths Medical CEO Jeffery McCaulley appeared first on MassDevice.



from MassDevice http://ift.tt/2cNw87B

NEST update: Recommendations for early-phase projects of US medical device evaluation system

Emergo GroupBy Stewart Eisenhart, Emergo Group

EMERGO SUMMARY OF KEY POINTS:

  • The FDA and other stakeholders are moving forward incrementally with their National Evaluation System for health Technology (NEST).
  • NEST managing boardmembers recommend demonstration projects as early-stage activities of the NEST program.
  • Recommended early-stage NEST projects focus on pre-and post-market evidence evaluations.

The planning board of a US Food and Drug Administration project to develop a nationwide evaluation and monitoring system for medical devices has issued new recommendations for implementing early-stage components of the program.

The latest report on the proposed National Evaluation System for health Technology (NEST) focuses on early-stage activities the program’s Coordinating Center should undertake in order to establish viable networks of data partners and sources, methodological expertise and best practices, and communication processes for both project participants and the public.

“The Planning Board recommends the Coordinating Center use demonstration projects as a way to develop these shared resources while also showing the value of a nationally coordinated approach to bridging efforts and closing the gaps in medical device evaluation,” the report states.

The report divides implementation of these demonstration projects into two phases. Phase one projects should include balancing pre- and postmarket device evidence development efforts, as well as improving safety surveillance of devices in order to eventually achieve an active national surveillance system.

Phase two project recommendations include boosting and improving data collection and integrating health technology systems for better Class II device regulatory evaluations; pushing more use of patient-mediated data sharing platforms; and devising ways to measure device value within the NEST infrastructure.

Manufactures whose devices are registered for sale in the US should keep track of NEST developments, as the eventual implementation of such a system will have significant effects on their FDA compliance requirements.

Stewart Eisenhart covers medical device regulatory affairs for Emergo Group.

The opinions expressed in this blog post are the author’s only and do not necessarily reflect those of MassDevice.com or its employees.

The post NEST update: Recommendations for early-phase projects of US medical device evaluation system appeared first on MassDevice.



from MassDevice http://ift.tt/2dtyRWB