Making machined parts for the medical industry is not like making parts for consumer goods. Whereas most ordinary metal parts must meet ISO 9001 quality management requirements, medical parts must meet further standards.

According to the International Standards Organization, companies involved in the design, development, production, storage, distribution, installation or servicing of medical parts must demonstrate their “ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.” The standard used to measure that ability is ISO 13485, which is recognized by regulators such as the FDA. Our network of vendors is certified for the said standards and can deliver the tightest of tolerances and precision need to serve the medical industry.