Medical Device Manufacturer · US , Round Rock , TX

Orthopro, LLC - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

Total

Cleared

Denied

Orthopro, LLC has 7 FDA 510(k) cleared medical devices. Based in Round Rock, US.

Historical record: 7 cleared submissions from 2006 to 2013. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Orthopro, LLC

7 devices

1-7 of 7