Medical Device Manufacturer · US , Miami , FL

Spineup, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2022
2
Total
2
Cleared
0
Denied

Spineup, Inc. has 2 FDA 510(k) cleared medical devices. Based in Miami, US.

Latest FDA clearance: May 2025. Active since 2022. Primary specialty: Orthopedic.

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

FDA 510(k) cleared devices by Spineup, Inc.

2 devices
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