Medical Device Manufacturer · FR , Wervicq-Sud

Cousin Biotech Sas - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2008

Total

Cleared

Denied

Cousin Biotech Sas has 6 FDA 510(k) cleared medical devices. Based in Wervicq-Sud, FR.

Historical record: 6 cleared submissions from 2008 to 2019. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Cousin Biotech Sas Filter by specialty or product code using the sidebar.

Cousin Biotech Sas 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 - Cousin Biotech Sas

6 devices

1-6 of 6