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Biodynamik, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K260073
XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mm
February 10, 2026
K241357
XT3 System
January 22, 2025