Medical Device Manufacturer · US , Memphis , TN

Danek Group, Inc. - FDA 510(k) Cleared Devices

2 submissions · 0 cleared · Since 1994

Total

Cleared

Denied

Danek Group, Inc. has 0 FDA 510(k) cleared medical devices. Based in Memphis, US.

Historical record: 0 cleared submissions from 1994 to 1995. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Danek Group, Inc.

2 devices

1-2 of 2