Vesalio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vesalio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: V-DAC Catheter, NeVa PV Thrombectomy Device, NeVasc Aspiration System
4
Total
3
Cleared
0
Denied
Vesalio, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Jan 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.
FDA 510(k) Regulatory Record - Vesalio, Inc.
4 devices