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Escala Medical, Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K260380
Mendit
March 4, 2026
K230730
Apyx
July 25, 2023
K213783
Apyx
April 5, 2022