FDA registration. You can also call it FDA registration. Refers to the cosmetics, medical devices, drugs, food, laser products exported to the United States must be put on record to the United States Federal Food and Drug Administration, and ensure that the products meet the relevant standards and health and safety requirements of the United States, some of the products must also be issued relevant testing to record success. For example, Class II and III clinical medical products must provide 510K documents before they can be registered with FDA.

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