
A researcher tests the Biofilm Disruption Device (BDD) on a metal disk at the lab of Garwood Medical Devices at the University of Buffalo. [Image courtesy of Douglas Levere / University at Buffalo]
Garwood is presently raising $3 million in a series B round and is engaged in another round of testing its Biofilm Disruption Device (BDD); company officials plan to submit an application to U.S. FDA next year, according to a University of Buffalo news release.
“Our goal is to eliminate the need for follow-up surgeries. We think we can wipe out infection-causing bacteria before trouble starts,” said Garwood Medical Devices CEO Wayne Bacon.
Get the full story on our sister site Medical Design & Outsourcing.
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