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Sonavex Receives FDA 510(k) Clearance for EchoMark & EchoMark LP Tissue Markers – Sonavex

By June 6, 2018May 22nd, 2025No Comments

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Sonavex, Inc., a privately held medical device company focused on improving surgical patient outcomes with point-of-care imaging technologies, announced today that it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its EchoMark and EchoMark LP soft tissue markers. 

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