Medical Device Manufacturer · US , Cambridge , MA

Dynagen, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

Total

Cleared

Denied

Dynagen, Inc. has 6 FDA 510(k) cleared medical devices. Based in Cambridge, US.

Historical record: 6 cleared submissions from 1992 to 1996. Primary specialty: Toxicology.

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

FDA 510(k) Regulatory Record - Dynagen, Inc.

6 devices

1-6 of 6