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Cg Medtech Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
4
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252351
UniSpace® TPLIF Cage
October 28, 2025
K251725
ANAX OCT Spinal System
June 25, 2025