Medical Device Manufacturer · US , Wilmington , DE

Greiner America, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1996

Total

Cleared

Denied

Greiner America, Inc. has 7 FDA 510(k) cleared medical devices. Based in Wilmington, US.

Historical record: 7 cleared submissions from 1996 to 1997. Primary specialty: Chemistry.

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

Greiner America, 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 America, Inc.

7 devices

1-7 of 7