Medical Device Manufacturer · US , Blue Ash , OH

Vein 360, LLC - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2019

Total

Cleared

Denied

Vein 360, LLC has 4 FDA 510(k) cleared medical devices. Based in Blue Ash, US.

Last cleared in 2023. Active since 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Vein 360, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Vein 360, LLC

4 devices

1-4 of 4