Medical Device Manufacturer · DE , Tuttlingen

Karl Storz SE & CO. KG - FDA 510(k) Cleared Devices

23 submissions · 23 cleared · Since 2018
23
Total
23
Cleared
0
Denied

Karl Storz SE & CO. KG has 23 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.

Latest FDA clearance: Mar 2026. Active since 2018. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Karl Storz SE & CO. KG Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Karl Storz SE & CO. KG

23 devices
1-12 of 23
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