Medical Device Manufacturer · US , Mission Viejo, , CA

Tenacore Holdings, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2002

Total

Cleared

Denied

Tenacore Holdings, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mission Viejo,, US.

Historical record: 4 cleared submissions from 2002 to 2008. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Tenacore Holdings, Inc.

4 devices

1-4 of 4