Medical Device Manufacturer · US , Olathe , KS

Ensite Vascular - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

Denied

Ensite Vascular has 2 FDA 510(k) cleared medical devices. Based in Olathe, US.

Last cleared in 2021. Active since 2019. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Ensite Vascular Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Ensite Vascular

2 devices

1-2 of 2