Medical Device Manufacturer · US , Andover , MA

Hager Worldwide, Inc. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2005

Total

Cleared

Denied

Hager Worldwide, Inc. has 3 FDA 510(k) cleared medical devices. Based in Andover, US.

Historical record: 3 cleared submissions from 2005 to 2006. Primary specialty: Dental.

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

Hager Worldwide, 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 - Hager Worldwide, Inc.

3 devices

1-3 of 3