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Medical Murray can help bring your medical device from concept all the way to distribution. Our team of biomedical, mechanical, quality & manufacturing engineers will support all the services required to design, develop, test, and manufacture your Class II and Class III medical device. 

We are certified to ISO 13485:2016 for both design and manufacturing and can handle all aspects of the complex FDA regulatory filing process for you.

There are three Medical Murray facilities in the U.S. - our H.Q. in North Barrington, IL, a manufacturing facility in Lake Zurich, IL, and a development facility in Charlotte, NC.

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