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As the EU’s 2017 Medical Device Regulation (MDR) comes fully into force, devicemakers need to keep track of significant changes in the form of “implementing and delegated acts,” according to one UK-based regulatory expert. Read More
Smiths Medical has issued an urgent medical device correction letter about a potential risk associated with pressure chambers used with the company’s Level 1 Fast Flow Fluid Warmers, which deliver solutions or warmed blood to patients. Read More
The Center for Devices and Radiological Health (CDRH) is seeking companies involved in medical device development and manufacturing to participate in its Experiential Learning Program (ELP), which sends CDRH staff on virtual or on-site training visits. Read More
Lice Clinics of America says its medical device is the only product on the market that has been cleared by the FDA to use air in treating head lice. Read More
Boston Scientific has agreed to pay $85 million to Nevro to settle their intellectual property litigation over spinal cord stimulation patents. Read More
The FDA has pledged to help manufacturers of sterilized devices if a new emissions regulation planned by the Environmental Protection Agency (EPA) for later this year causes disruption in commercial sterilizer facility operations. Read More
A patent that Magnolia Medical Technologies holds for its Steripath blood specimen diversion device for blood tests is valid, and competitor Kurin owes the company $2.1 million in royalties, according to a federal court verdict. Read More
Conmed is expanding its implant portfolio with the purchase of Biorez, a Connecticut-based start-up that focuses on soft tissue healing technology. Read More