Warmest congratulations to our company for obtaining FDA certification for our diode laser equipment.

In June 2025, our independently developed and manufactured diode laser equipment received FDA-510k approval from the U.S. Food and Drug Administration (FDA), registration certificate number: 21 CFR 878.4810. This means that the product can be legally distributed in the U.S. market, laying a solid foundation for our global market presence in the medical industry and marking another important milestone in our internationalization strategy, accelerating the company's global expansion.