Medical Device Manufacturer · FR , Montpellier

Medtech S.A.S - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2010

Total

Cleared

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) cleared devices by Medtech S.A.S

3 devices

1-3 of 3