C.G. Laboratories, Inc. specializes in the validation and development of Manufacturer’s Instructions for Use (IFU) for Reusable Medical Devices. As per FDA regulations, the responsibility for testing and validating any labeling claims for reuse provided in the IFU rests with the device manufacturer. Our Laboratory Department, which is certified by ISO 13485:2016, is a well-equipped facility with a team that collectively has over 90 years of experience in serving the medical device industry. At C.G. Laboratories, Inc., we are dedicated to upholding sound scientific principles.