At MedPlast, we understand that we’re not just manufacturing products—we’re making components and finished devices that will be used to save or enhance a patient’s life. That’s why we’re committed to achieving the highest standards of quality in everything we do.
With 35+ years of medical device experience, we have developed a thorough understanding of the complex regulatory environment. Every product is manufactured to exact specification, in full compliance with FDA guidelines, at one of our ISO 13485 certified facilities. Additionally, our single global quality vision and policy is designed to ensure consistent high quality and compliance at every location, on every project, at every stage of the product lifecycle.
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