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I-Tek Medical Technologies is an industry leader for contract development and manufacturing. I-Tek offers an extensive range of medical device manufacturing services starting at early conception through prototyping and on to sterilization validation coordination with project management throughout the entire process.

We operate in an FDA GMP compliant facility with ISO 13485:2003 certification. I-Tek employees are experts in medical device development and commercialization allowing our customers to receive the highest quality service in a rapid and cost effective manner.

The I-Tek facility includes Class 7 (10,000) and Class 5 (100) Clean room manufacturing environments as well as cost efficient white room manufacturing areas. Our facility is equipped to manufacture and package your device in a manner that will exceed your expectations. Our personnel are trained and certified to work in each and all of the areas of manufacturing. With over 100 years of combined contract services experience the I-Tek team has collectively designed, developed and commercialized over 150 medical devices. From Class I to Class III devices, we understand the technical challenges of research and development along with the regulatory hurdles required to release products to commercialization.

If your goal is to decrease development time, increase speed to market, obtain assistance with product design, and partner with a credible, experienced medical manufacturing team, then I-Tek Medical Technologies is your solution.

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