Medical Device Manufacturer · FR , Montpellier

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

8 submissions · 8 cleared · Since 2009

Total

Cleared

Denied

Medtech S.A has 8 FDA 510(k) cleared medical devices. Based in Montpellier, FR.

Historical record: 8 cleared submissions from 2009 to 2020. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Medtech S.A Filter by specialty or product code using the sidebar.

Medtech S.A is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Medtech S.A

8 devices

1-8 of 8