Medical Device Manufacturer · US , Round Rock , TX

Verticor, Ltd. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

Verticor, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Round Rock, US.

Historical record: 3 cleared submissions from 2009 to 2011. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Verticor, Ltd.

3 devices

1-3 of 3