Our industry-recognized medical device design experience is sustained by a team of over eighty talented mechanical engineering, electrical engineering, software engineering and systems engineering experts. KMC’s contract engineering services follow a robust stage-gate process throughout the entire product life cycle with a focus on the reliability, manufacturability, testability and serviceability of a product design. Our robust quality management system complies with the FDA’s Quality Systems Regulation 21 CFR Parts 820, 803 and 806, as well as ISO 13485:2003.