For over 25 years, Teco Diagnostics has been an industry leader in the manufacturing of in-vitro diagnostics and medical devices. From urinalysis to clinical chemistry reagents, we have high quality solutions for all diagnostics needs. Based in the USA with a 40,000 square foot facility in Anaheim, CA, our manufacturing is FDA regulated, with all phases of our production processes based on strict Current Good Manufacturing Practices (CGMP) regulations. In addition, our ISO 13485 certification ensures that Teco meets the international quality management systems standard for medical device companies. With customers and distributors in over 100 countries worldwide and CE marking and established registration already available, we take great pride in being able to service the world with our products.
PRESIDENT / FOUNDER / DIRECTOR OF RESEARCH AND DEVELOPMENT
Graduate School and Degree
PhD in Toxicology from University of Kentucky
Dr. KC Chen, Founder and President of Teco Diagnostics, oversees the R&D and quality systems departments. Dr. Chen has over 27 years of manufacturing and sales experience in the in-vitro diagnostics industry. Under Dr. Chen’s leadership, Teco Diagnostics recently celebrated its 27th year in business and is recognized worldwide as a high quality US manufacturer of in-vitro diagnostic test kits. Previous to Teco Diagnostics, Dr. Chen worked as an R&D scientist at General Motors. Dr. Chen holds a PhD in toxicology from the University of Kentucky.