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/ EMA Aesthetics , Ltd.
EMA Aesthetics , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K243055
Préime DermaFacial Collagen+
April 15, 2025
K243072
Préime DermaFacial (MicroT)
April 1, 2025