Karl Storz Endovision, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Karl Storz Endovision, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Karl Storz Endovision, Inc. has 1 FDA 510(k) cleared medical devices. Based in Charlton, US.
Latest FDA clearance: Jun 2024. Active since 2024. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Karl Storz Endovision, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Karl Storz Endoscopy America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Karl Storz Endovision, Inc.
1 devices