Medical Device Manufacturer · US , San Diego , CA

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

5 submissions · 4 cleared · Since 2025

Total

Cleared

Denied

Vesalio, Inc. has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.

Latest FDA clearance: Aug 2026. Active since 2025. Primary specialty: Cardiovascular.

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

Vesalio, Inc. is one of 16115 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5