Medical Device Manufacturer · US , Saugus , MA

Neoligaments, Ltd. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1990

Total

Cleared

Denied

Neoligaments, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Saugus, US.

Historical record: 7 cleared submissions from 1990 to 1995. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Neoligaments, Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Neoligaments, Ltd.

7 devices

1-7 of 7