Medical Device Manufacturer · US , Los Angeles , CA

Karl Storz Endoscopy America - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2020

Total

Cleared

Denied

Karl Storz Endoscopy America has 5 FDA 510(k) cleared medical devices. Based in Los Angeles, US.

Last cleared in 2022. Active since 2020. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Karl Storz Endoscopy America Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Karl Storz Endoscopy America

5 devices

1-5 of 5