Medical Device Manufacturer · US , Blue Ash , OH

Ethicon Endo-Surgery - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

Ethicon Endo-Surgery has 2 FDA 510(k) cleared medical devices. Based in Blue Ash, US.

Last cleared in 2023. Active since 2012. Primary specialty: General & Plastic Surgery.

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

FDA 510(k) cleared devices by Ethicon Endo-Surgery

3 devices

1-3 of 3