C.G. Laboratories has a new Washer Disinfector validated to ISO 15883 and is fully customizable to any cycle requirement.

FDA guidance document: Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling:

The FDA has identified specific medical devices that pose a greater likelihood of microbial transmission and pose a higher risk of infection if they are not adequately reprocessed. Let C.G. Laboratories assist you in making the right determination for your specific product. Our Scientists have comprehensive solutions to fit all of your reprocessing needs.

C.G. Laboratories, Inc.

(817) 270-1945

Why Choose CG Laboratories?

C.G. Labs began in 1983 as a microbiology laboratory founded by Dr. Glenn Crum. In 1996, we relocated to Granbury, TX and expanded our services to include medical device contract manufacturing. We have grown into a multi-service company with three distinct divisions with 19,000 square feet spanning two sites. All our services are current, regulated and quality-driven. We are registered with the FDA and ISO accredited to 13485:2016 and MDSAP.

Our GET MORE objective gives you great customer service, guidance, quality management and access to experts. We strive to exceed your expectations, to meet government regulations and to make the world a safer place. With C.G. Laboratories, you always GET MORE.