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PHOMED is proud to announce that on March 19, 2026, our medical device products officially received U.S. FDA clearance, marking an important milestone in the company's international development and regulatory compliance journey.
Receiving FDA clearance demonstrates that our products have successfully met the applicable U.S. regulatory requirements for safety, quality, and performance. It also reflects PHOMED's long-term commitment to technological innovation, product quality, and compliance with internationally recognized standards.
For nearly 20 years, PHOMED has specialized in the research, development, manufacturing, and global distribution of medical laser systems for rehabilitation therapy, minimally invasive surgery, dental applications, and veterinary medicine. Throughout this journey, we have remained committed to providing reliable medical solutions for healthcare professionals worldwide.
This achievement not only strengthens our ability to serve customers in the United States but also further supports our global partners with products that meet internationally recognized regulatory standards.
We would like to express our sincere appreciation to our customers, distributors, clinical partners, and every member of the PHOMED team whose trust and dedication have made this milestone possible.
Looking ahead, PHOMED will continue investing in research and development, expanding our product portfolio, and delivering innovative, high-quality medical laser solutions to customers around the world.
Together, we look forward to shaping the future of medical laser technology.
