Medical Device Manufacturer · US , Saratoga , CA

CapsoVision, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2016

Total

Cleared

Denied

CapsoVision, Inc. has 7 FDA 510(k) cleared medical devices. Based in Saratoga, US.

Latest FDA clearance: Sep 2026. Active since 2016. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by CapsoVision, Inc. Filter by specialty or product code using the sidebar.

CapsoVision, Inc. is one of 16149 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - CapsoVision, Inc.

7 devices

1-7 of 7