Medical Device Manufacturer · US , Walker , MI

Durden Enterprises, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1984

Total

Cleared

Denied

Durden Enterprises, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 4 cleared submissions from 1984 to 1991. Primary specialty: Neurology.

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

Durden Enterprises, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Durden Enterprises, Inc.

4 devices

1-4 of 4