Medical Device Manufacturer · US , Blue Ash , OH

Ethicon Endo-Sugery, LLC - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2008

Total

Cleared

Denied

Ethicon Endo-Sugery, LLC has 6 FDA 510(k) cleared medical devices. Based in Blue Ash, US.

Historical record: 6 cleared submissions from 2008 to 2011. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Ethicon Endo-Sugery, LLC Filter by specialty or product code using the sidebar.

Ethicon Endo-Sugery, LLC is one of 20278 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Ethicon Endo-Sugery, LLC

6 devices

1-6 of 6