Medical Device Manufacturer · FR , Toulouse

Sudimplant SA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2006

Total

Cleared

Denied

Sudimplant SA has 2 FDA 510(k) cleared medical devices. Based in Toulouse, FR.

Historical record: 2 cleared submissions from 2006 to 2007. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Sudimplant SA Filter by specialty or product code using the sidebar.

Sudimplant SA 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 - Sudimplant SA

2 devices

1-2 of 2