Medical Device Manufacturer · CA , Montreal

Co-Ligne AG - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Co-Ligne AG has 4 FDA 510(k) cleared medical devices. Based in Montreal, CA.

Historical record: 4 cleared submissions from 2004 to 2009. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Co-Ligne AG Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Co-Ligne AG

4 devices

1-4 of 4