Medical Device Manufacturer · US , Niagara Falls , NY

Bip USA, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1993

Total

Cleared

Denied

Bip USA, Inc. has 7 FDA 510(k) cleared medical devices. Based in Niagara Falls, US.

Historical record: 7 cleared submissions from 1993 to 2003. Primary specialty: General & Plastic Surgery.

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

Bip USA, 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 - Bip USA, Inc.

7 devices

1-7 of 7