Spine Innovation, LLC

FDA Regulatory Profile

Spine Innovation, LLC appears in FDA public data with 0 recalls, 2 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 8, 2026.

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