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Shenzhen Lifotronic Technology Co., Ltd.

FDA Regulatory Profile

Shenzhen Lifotronic Technology Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 30, 2025.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251076Diode Laser Hair Removal Machine (models: T60A, T60B, T60C, T60D, T60E)July 30, 2025
K192466Air Compression Therapy SystemJune 22, 2020

FDA data resources