Lemaitre Vascular is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lemaitre Vascular - FDA 510(k) Cleared Devices
Recent clearances: XenoSure Biologic Patch, EZE SIT Valvulotome, Pruitt F3 Carotid Shunt, 10 Fr, Pruitt F3 Carotid Shunt, 9 Fr, Pruitt F3 Carotid Shunt, 8 Fr
3
Total
3
Cleared
0
Denied
Lemaitre Vascular has 3 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 3 cleared submissions from 2018 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lemaitre Vascular Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lemaitre Vascular
3 devices