Vena Group, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vena Group, LLC - FDA 510(k) Cleared Devices
Recent clearances: VenaOne
1
Total
1
Cleared
0
Denied
Vena Group, LLC has 1 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Vena Group, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jkh USA, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Vena Group, LLC
1 devices