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Spine Innovation, LLC

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K253266Titanium Interbody SystemJanuary 8, 2026
K153356Spine Innovation Interbody SystemJanuary 14, 2016