Medical Device Manufacturer · US , Danbury , CT

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

7 submissions · 7 cleared · Since 2005

Recent clearances: Compex HD

Total

Cleared

Denied

Addent, Inc. has 7 FDA 510(k) cleared medical devices. Based in Danbury, US.

Historical record: 7 cleared submissions from 2005 to 2019. Primary specialty: Dental.

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

Addent, 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 - Addent, Inc.

7 devices

1-7 of 7