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.

Karl Storz Endoscopy America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5