Medical Device Manufacturer · US , Eden Prairie , MN

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

3 submissions · 3 cleared · Since 2005

Total

Cleared

Denied

Celleration, Inc. has 3 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.

Historical record: 3 cleared submissions from 2005 to 2014. Primary specialty: General & Plastic Surgery.

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

Celleration, Inc. is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Celleration, Inc. — FDA 510(k) Products and Clearance History

3 devices

1-3 of 3