Hello! For what products in the Amazon need FDA registration / certification, the U.S. FDA has the following requirements:
China and the U.S. on the definition of food, drugs, medical devices, radiation electronic products, cosmetics is different, resulting in the United States of America in the scope of these products is different from the domestic. At present, hand disinfection products, toothbrushes, dental floss, laser rangefinders and ultrasonic humidifiers and other radiation-based electronic products, pharmaceuticals and food ingredients that need to be further processed into finished products are under the jurisdiction of the U.S. FDA. Therefore, enterprises must be necessary before exporting to the United States to register or record, a lot of domestic enterprises because they do not understand these and lead to the FDA refused entry or even be added to the blacklist.
It should be noted that the registration is necessary, but does not mean that the FDA certified these products. Products currently certified and approved by the FDA include new drugs, generic drugs, and most Class III medical devices (e.g., artificial hearts).
Additional science: What is FDA approval?
The FDA stands for Food and Drug Administration. To be precise, the U.S. FDA does not do most of the products certified, but companies must do the record or registration, otherwise the U.S. FDA has the right to take action on the goods, including the goods detained, refused entry or even destroyed, the company was added to the blacklist. Products subject to the jurisdiction of the U.S. FDA are food, food contact materials, drugs, pharmaceutical ingredients, cosmetics, medical devices, radiation-based electronic products, tobacco products, before entering the U.S., companies need to make the necessary registration. For more information about FDA certification, please contact us at #Registrar Corp#
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