We have a rich heritage in the field of medical devices, having conducted extensive testing on numerous innovative products available today to ensure their safety and effectiveness. The U.S. Federal Food, Drug, and Cosmetic Act (FD&C Act) of 1938 marked a significant milestone, initiating government oversight of medical devices in the United States. Subsequently, the Cooper Committee was commissioned by the U.S. Congress to conduct a comprehensive inventory of all existing medical devices. As a result of this review, the 1976 Medical Device Amendments were enacted, granting regulatory authority to the U.S. FDA for overseeing medical devices. This pivotal moment brought about substantial changes in the medical device industry and laid the foundation for the establishment of Medisol Laboratories.
Our dedicated team comprises more than 500 scientists, technicians, and service specialists who diligently carry out over 800 rigorous tests across 13 global laboratory locations. With decades of unparalleled expertise, we take pride in the quality of our outcomes and the strong partnerships we foster with our valued customers.