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Spineup, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K250446Frida™ Anterior Cervical Plate SystemMay 23, 2025
K212358Romero Cervical CageJanuary 10, 2022