Medical Device Manufacturer · US , Cambridge , MA

Etex Co. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1992

Total

Cleared

Denied

Etex Co. has 2 FDA 510(k) cleared medical devices. Based in Cambridge, US.

Historical record: 2 cleared submissions from 1992 to 1993. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Etex Co.

2 devices

1-2 of 2