Ensite Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ensite Vascular - FDA 510(k) Cleared Devices
Recent clearances: SiteSeal SV, Site Seal SV
2
Total
2
Cleared
0
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.
Regulatory submissions have been managed by TAMM Net, Inc. and Brosseau Consulting, LLC.
FDA 510(k) Regulatory Record - Ensite Vascular
2 devices