Lutronic Aesthetic

FDA Regulatory Profile

Lutronic Aesthetic appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jan 2, 2024.

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Summary

Total Recalls
0
510(k) Clearances
1
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K233550MOSAIC 3D (Surgical Laser)Jan 2, 2024