← Every applicant

Sanhe LEFIS Electronics Co., Ltd. FDA Approvals

0 new drug approvals and 4 device clearances on file. This applicant is not matched to a listed company.

Newest first

A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.

Product
Diode Laser Therapy System510(k)Sep 10, 2026General, Plastic Surgery
Intense Pulsed Light Therapy Device510(k)Jun 12, 2026General, Plastic Surgery
CO2 Laser Therapy System (Model: LFS-D9U)510(k)Dec 19, 2025General, Plastic Surgery
Q-Switched Nd: YAG Laser machine (LFS-C13U)510(k)Oct 20, 2025General, Plastic Surgery

Related datasets