Ethicon Endo-Surgery, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ethicon Endo-Surgery, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ECHELON FLEX POWERED VASCULAR STAPLER WITH ADVANCED PLACEMENT TIP, ENDOPATH ECHELON VASCULAR WHITE RELOADS FOR ADVANCED, VALUTRUS REUSABLE CIRCULAR STAPLER AND DISPOSABLE RELOADS, ECHELON FLEX 45 / 60 POWERED ARTICULATING ENDOSCOPIC LINEAR CUTTER
Ethicon Endo-Surgery, Inc. has 112 FDA 510(k) cleared general & plastic surgery devices. Based in Cincinnati, US.
Historical record: 112 cleared submissions from 1992 to 2014.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Tuv Product Service, Inc. and Ethicon Endo Surgery, Inc..
FDA 510(k) Regulatory Record - Ethicon Endo-Surgery, Inc.
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