Sanhe?Lefis?Electronics?Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Diode Laser Therapy System, Intense Pulsed Light Therapy Device, CO2 Laser Therapy System (Model: LFS-D9U)
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sanhe?Lefis?Electronics?Co., Ltd. General & Plastic Surgery ✕
4 devices
Cleared
Sep 10, 2026
Diode Laser Therapy System
General & Plastic Surgery
122d
Cleared
Jun 12, 2026
Intense Pulsed Light Therapy Device
General & Plastic Surgery
60d
Cleared
Dec 19, 2025
CO2 Laser Therapy System (Model: LFS-D9U)
General & Plastic Surgery
262d
Cleared
Oct 20, 2025
Q-Switched Nd: YAG Laser machine (LFS-C13U)
General & Plastic Surgery
87d