What does "FDA approved for export to the US" mean?

To be precise, there is no such thing as FDA certification. Usually people say FDA certification mainly refers to FDA registration (FDA Rregistrarion). The U.S. Food and Drug Administration, referred to as the FDA, has jurisdiction over products such as food, drugs, medical devices, cosmetics, radiation electronics, etc. The FDA adopts post-market supervision of all enterprises, i.e., an enterprise can first be registered with the FDA and exported. During the export process, the FDA will regulate compliance through customs sampling, factory inspections, foreign supplier verification programs, and other measures. The U.S. Food and Drug Administration (Food and Drug Administration) is referred to as the FDA, and the FDA is one of the executive agencies established by the U.S. government in the Department of Health and Human Services (DHHS) and the Department of Public **** Health (PHS). As a scientific regulatory agency, FDA's responsibility is to ensure the safety of food, cosmetics, drugs, biologicals, medical devices, and radiological products manufactured in or imported into the United States, including products that emit radiation, combination products, and other electronic and medical products that are related to personal health and safety. It was one of the first federal agencies to have consumer protection as its primary function.