Medical Device Manufacturer · US , Danbury , CT

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

7 submissions · 7 cleared · Since 2005

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.

FDA 510(k) cleared devices by Addent, Inc.

7 devices

1-7 of 7