Vein 360 is one of 25895 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vein 360 - FDA 510(k) Cleared Devices
Recent clearances: Vein360 Reprocessed LithoVue Digital Flexible Ureteroscope (Standard Deflection)
1
Total
1
Cleared
0
Denied
Vein 360 has 1 FDA 510(k) cleared medical devices. Based in Cincinnati, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vein 360 Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vein 360
1 devices