Arthex, Inc.

FDA Regulatory Profile

Arthex, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 24, 2023.

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