Medical Device Manufacturer · US , Minneapolis , MN

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

4 submissions · 4 cleared · Since 2001

Total

Cleared

Denied

Medafor, Inc. has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 4 cleared submissions from 2001 to 2013. Primary specialty: General & Plastic Surgery.

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

Medafor, Inc. is one of 5297 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Medafor, Inc. — FDA 510(k) Products and Clearance History

4 devices

1-4 of 4