Medical Device Manufacturer · US , American Fork , UT

Sanacor - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2007

Total

Cleared

Denied

Sanacor has 3 FDA 510(k) cleared medical devices. Based in American Fork, US.

Historical record: 3 cleared submissions from 2007 to 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Sanacor

3 devices

1-3 of 3