Knight Dental Group, Inc. is in compliance with the Food, Drug and Cosmetic Act of 1978 as referenced in Food and Drug Administration (FDA) (Code for Federal Regulations (CFR), Chapter 21, Section 801 as it relates to disclosure of manufacture of origin and patient contact materials.
Knight Dental Group, Inc. is in compliance with all Current Good Manufacturing Practices (CGMP) as outlined in the Food and Drug Administration (FDA) Code of Federal Regulations (CFR), Chapter 21, section 820, as it relates to design, manufacture, packaging, labeling and servicing of all finished devices intended for human use. Knight Dental Group is a ISO 13485 Quality Management System certified (US 12/82593) and a Dental Appliance Manufacturing Audit System (DAMAS) quality certified (#0505/0006) manufacturer of dental devices and is subject to third party audits.