Sanhe Lefis Electronics Co., Ltd.

FDA Regulatory Profile

Sanhe Lefis Electronics Co., Ltd. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 10, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K261562Diode Laser Therapy SystemSeptember 10, 2026
K261204Intense Pulsed Light Therapy DeviceJune 12, 2026
K250998CO2 Laser Therapy System (Model: LFS-D9U)December 19, 2025
K252319Q-Switched Nd: YAG Laser machine (LFS-C13U)October 20, 2025