Vesatek, LLC is one of 13331 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, Firebow 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.
510(k) submissions have been managed by Paul Gasser as regulatory consultant.
FDA 510(k) Regulatory Record - Vesatek, LLC
2 devices