Medical Device Manufacturer · US , Cottage Grove , MN

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

7 submissions · 7 cleared · Since 1985

Total

Cleared

Denied

Orthofab, Inc. has 7 FDA 510(k) cleared medical devices. Based in Cottage Grove, US.

Historical record: 7 cleared submissions from 1985 to 1997. Primary specialty: Physical Medicine.

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

Orthofab, Inc. is one of 14210 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7