Medtech S.A.S is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Medtech S.A.S - FDA 510(k) Cleared Devices
Recent clearances: ROSA ONE Brain Application, ROSA ONE Brain application
3
Total
3
Cleared
0
Denied
Medtech S.A.S has 3 FDA 510(k) cleared medical devices. Based in Montpellier, FR.
Last cleared in 2023. Active since 2010. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Medtech S.A.S Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtech S.A.S
3 devices