Medical Device Manufacturer · US , Marietta , GA

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

5 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Mimedx Group, Inc. has 2 FDA 510(k) cleared medical devices. Based in Marietta, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.

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

Mimedx Group, 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 - Mimedx Group, Inc.

5 devices

1-5 of 5