A cadre of insurers and other healthcare stakeholders urges the FDA to establish more registries to monitor and report performance of medical device on the U.S. market.
MASSDEVICE ON CALL — Some major healthcare industry players are looking to the FDA to provide more robust surveillance of medical devices on the U.S. market.
The group asked the FDA to look over a handful of recommendations for boosting medtech registries to gather more robust information about devices that have already been approved or cleared, saying that such measures could track safety issues.
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