Founded in 2004 as a division of Interplex Industries…our focus is 100% dedicated on the design, development and manufacture of next generation medical devices for OEM’s and startups. We maintain ISO 13485 certification and FDA registration in Design Control and as a contract manufacturer. Interplex Medical partners with our clients at the earliest stages of the product development process–including voice-of-the-customer research in a clinical setting–to develop the product input document for our client’s medical device.
Interplex Industries was established in 1958 and has five ISO 13485 certified facilities around the globe that can provide a seamless transition from US design, to off-shore or near-shore manufacturing. Thus, as a division of Interplex Industries, we have the ability to execute manufacturing transfer programs into a global facility that meets supply-chain and continual cost improvement requirements.
Interplex Medical utilizes a robust product development process that serves clients at all stages of their product life-cycle. We accomplish this by providing quick-turn functional prototypes to pre-production short-run clinical studies, including execution of design verification and process validation activities.
Interplex Medical is globally integrated with established facilities in fourteen cities across the United States, Mexico, Europe and Asia. With this global presence, OEM’s can count on a seamless integration of manufacturing services that result in less time-to-market for all of their products.
Interplex Medical is unmatched when it comes to clinical knowledge and proven engineering expertise. We combine this award-winning innovation to produce enabling solutions in all facets of medical device design.