GUIDEPATH MEDICAL partners with physicians and medical device companies to clearly define desired clinical outcomes and design inputs. Then, based upon our breadth of experience in polymers, metals, and coatings, we drive products through prototyping, regulatory submissions then into manufacturing. We rely on a collaborative and nimble project integration approach which allows for information sharing across sites and across borders. Guidepath reliably moves products from design into production, allowing devices to quickly get to market.

Guidepath adheres to design control per FDA CFR requirements, ISO 13485 and ISO 9001.

If you would like to discuss design possibilities with Guidepath, please contact