Martech® Medical Products is an FDA Registered Medical Device Manufacturer and ISO 13485:2003 registered company. All facilities comply with all FDA QSR and ISO requirements for manufacturing medical devices. Martech® Medical has an experienced Regulatory Department that can assist with all phases of international product approvals, including FDA 510(k) and PMA, EU-CE, Canadian Licensing, and Japanese Shonin.
Martech provides concept to production services and support to the top medical device companies in the world. With three manufacturing and engineering facilities, over 2,000 employees and 200,000 square feet of manufacturing space we develop and produce the highest quality medical devices for use around the world. Our ability to complete projects, from small to large, uniquely positions Martech to serve all customers. Services that smaller companies do not have or larger companies do not wish to spare, Martech can deliver and always works for you.