Medical Device Manufacturer · US , Monroe , NC

Greiner Bio-One Na, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2016

Total

Cleared

Denied

Greiner Bio-One Na, Inc. has 5 FDA 510(k) cleared medical devices. Based in Monroe, US.

Historical record: 5 cleared submissions from 2016 to 2019. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Greiner Bio-One Na, Inc. Filter by specialty or product code using the sidebar.

Greiner Bio-One Na, 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 - Greiner Bio-One Na, Inc.

5 devices

1-5 of 5