Vantis Vascular, Inc. is one of 16075 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vantis Vascular, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CrossFAST Integrated Microcatheter Advanced Delivery System, CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)
2
Total
2
Cleared
0
Denied
Vantis Vascular, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Sep 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vantis Vascular, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vantis Vascular, Inc.
2 devices