Medical Device Manufacturer · FR , Le Plessis Robinson Cedex

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

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Porges S.A. has 4 FDA 510(k) cleared medical devices. Based in Le Plessis Robinson Cedex, FR.

Historical record: 4 cleared submissions from 2001 to 2002. Primary specialty: Gastroenterology & Urology.

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

Porges 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 - Porges S.A.

4 devices

1-4 of 4