Spineup, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Spineup, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Frida™ Anterior Cervical Plate System, Romero Cervical Cage
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) Regulatory Record - Spineup, Inc.
2 devices