Medical Device Manufacturer · US , Westmont , IL

SpineCraft - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2009

Total

Cleared

Denied

SpineCraft has 3 FDA 510(k) cleared medical devices. Based in Westmont, US.

Latest FDA clearance: Apr 2026. Active since 2009. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - SpineCraft

3 devices

1-3 of 3