Steri-Tek Information

SteriTek is a high-volume E-beam/X-ray contract sterilizer and R&D innovation center serving the medical device, biotech, pharmaceutical and other industries. Steri-Tek is ISO 11137 and ISO 13485 certified, FDA registered, DEA registered as well as State of California Medical Device and Drug Manufacturing licensed facility. Our new facility in Lewisville(Dallas area) Texas will be opening October 2022. The facility boasts two state-of-the-art 10 MeV, 20 KW linear accelerators, opposite each other along the conveyor to provide uniform dose to the product without having to rotate the customer’s boxes. This dual-beam configuration significantly increases efficiencies, expands product options, and serves as an effective back-up for the accelerators. The facility provides the most 10 MeV sterilization capacity, the most comprehensive product options, and the highest uptime availability than any other facility in North America. SteriTek offers a seamless dose map validation of customer’s product from any other contract irradiator. Our staff of validation engineers provide expert consultation for setting up any products to be dose mapped. We also offer turnkey sterilization validations for any new products to be introduced into the market at some of the most competitive rates. Call 510.933.9700 today to learn more about how SteriTek can help you with your medical devices, pharmaceuticals, material modification, and food safety.