FDA Certification is a common search term used by businesses seeking to meet United States Food and Drug Administration requirements. However, the FDA does not issue one general certification that applies to every product. Requirements vary depending on whether a business manufactures food, drugs, medical devices, cosmetics, or other regulated products. Depending on the product, businesses may need to complete registration, listing, premarket review, or other regulatory steps. For example, some medical devices require FDA clearance or approval before marketing, while registration alone does not mean that a product has been approved. Understanding the relevant FDA requirements helps manufacturers prepare appropriate documentation, manage quality controls, and plan market entry. Businesses should identify the rules that apply to their products before advertising them as FDA certified.