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Curvafix, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252019CurvaFix Low Profile SystemAugust 29, 2025
K222505CurvaFix IM SystemOctober 27, 2022
K180050CurvaFix Intramedullary Rodscrew SystemMarch 1, 2019