From the first day of business in 1975 and every day since, quality has been given the highest priority at Wytech. Wytech is fully committed to a company-wide quality system that meets the stringent requirements of the medical device industry. This includes integrating lean enterprise principles for continuous improvement, eliminating waste, and streamlining processes, with the goal of producing safe products with zero defects. In addition, Wytech provides first article inspection and process validation if specified by our customers. Certificates documenting manufacturing specifications, dimensions, alloy chemistry, and mechanical test results are available upon request.
Ensuring the quality of Wytech’s products requires attention to precise manufacturing of diameters, lengths, and other specifications within tolerances of ten thousandths of an inch. Wytech’s quality systems provide for the prevention and detection of non-conforming parts, supported by a large scope of QC instrumentation as well as expertise in visual inspection. When a non-conformance part is detected, prompt corrective action is taken.
ISO 9001:2015 and ISO 13485:2016 Certified
Wytech Industries, Inc. has been assessed and certified as meeting the requirements of ISO 9001:2015 and ISO 13485:2016 for the manufacture of fine wire and tubing components for use in medical devices and other applications (excluding product design). Please click below to view our certificates.
FDA Registration #3003498655
Wytech Industries is a Qmed Qualified Supplier to the medical device industry. Click here for more information.