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Arthex, Inc.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K223759Arthrex SynergyID Endoscopic Imaging SystemFebruary 24, 2023
K172612FiberTak DXSeptember 28, 2017
K151256Arthrex BioSync® Bone WedgeAugust 12, 2015