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Acteev Biodefend’s™

Surgical Mask in Development With Acteev™ Technology Shows Efficacy Against SARS-CoV-2 Plus Level III Filtration Properties

Ascend Performance Materials announced today it has submitted to the U.S. Food and Drug Administration a 510(k) premarket notification for clearance to market its ActeevTM technology in a pair of high-efficacy surgical masks to protect against SARS-CoV-2, the cause of COVID-19.

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The XyCAM RI

U.S. Food & Drug Administration Grants 510(k) Clearance For Vasoptic Medical's Retinal Imaging Device

Vasoptic Medical Inc., a Maryland-based medical device company, announced that the company received 510(k) clearance from the U.S. Food & Drug Administration to market its XyCAM RI™—a non-invasive retinal imager designed to capture and provide dynamic blood flow information for clinical use.

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