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Ziehm-Orthoscan, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K252579
Orthoscan TAU MVP Mini C-Arm System
January 14, 2026
K250587
Orthoscan TAU Mini C-Arm
July 2, 2025
K243452
Orthoscan VERSA Mini C-Arm
January 14, 2025