Medical Device Manufacturer · US , Irvine , CA

Synovis Orthopedic & Woundcare - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Synovis Orthopedic & Woundcare has 3 FDA 510(k) cleared medical devices. Based in Irvine, US.

Historical record: 3 cleared submissions from 2011 to 2012. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Synovis Orthopedic & Woundcare Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Synovis Orthopedic & Woundcare

3 devices

1-3 of 3