Medical Device Manufacturer · US , Allentown , PA

The Traumafuse Co. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1989

Total

Cleared

Denied

The Traumafuse Co. has 4 FDA 510(k) cleared medical devices. Based in Allentown, US.

Historical record: 4 cleared submissions from 1989 to 1990. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - The Traumafuse Co.

4 devices

1-4 of 4