Huadong Medicine Co.,Ltd. (SHE: 000963) has announced that its wholly-owned subsidiary, Viora Ltd., has obtained the Medical Device Registration Certificate from China's National Medical Products Administration (NMPA) for its Class III medical device, the skin treatment system V30. The approval was granted on June 24, 2026.
The V30 device, developed by Viora, is an integrated skin treatment platform combining radiofrequency (RF), intense pulsed light (IPL), and Nd:YAG laser energy sources. It incorporates proprietary technologies, including CORE™ bipolar RF and PCR™ IPL, and can be equipped with various specialized handpieces for IPL, RF, and laser treatments. The system is designed to offer customizable treatment regimens tailored to different skin types and concerns, providing comprehensive solutions for the face, neck, and body. Its applications include reducing wrinkles, hair removal, and treating vascular and pigmented lesions, as well as acne.
The V-Series products are noted for their strong compatibility, allowing for integration with new technologies Viora may develop in the future. The V30 model has previously received registration approvals from the U.S. Food and Drug Administration (FDA) and the European Union's CE marking. Another product in the same series, the V20 (branded as Renotion in English), received NMPA approval for market launch in September 2024.
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