Vesatek, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vesatek, LLC - FDA 510(k) Cleared Devices
Recent clearances: LiteSaber Wire Torque Assist Device
2
Total
2
Cleared
0
Denied
Vesatek, LLC has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 2017 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vesatek, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vesatek, LLC
2 devices