Vexim SA is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Vexim SA - FDA 510(k) Cleared Devices
Recent clearances: SpineJack Expansion Kit
1
Total
1
Cleared
0
Denied
Vexim SA has 1 FDA 510(k) cleared medical devices. Based in Balma, FR.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Vexim SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
FDA 510(k) Regulatory Record - Vexim SA
1 devices