For over 30 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.