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.

SpineCraft is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - SpineCraft

3 devices

1-3 of 3