The US FDA is the abbreviation of Food and Drug Administration, which is the US Food and Drug Administration. To be precise, the U.S. FDA does not certify most products, but companies must file or register. Otherwise, the U.S. FDA has the right to take action against the goods, including detaining the goods, refusing entry or even destroying them, and adding companies to the blacklist. Products subject to the jurisdiction of the U.S. FDA include food, food contact materials, drugs, pharmaceutical ingredients, cosmetics, medical devices, radiation electronic products, and tobacco products. Before entering the United States, companies must complete necessary registrations.
China and the United States have different definitions of food, medicine, medical equipment, radiation electronic products, and cosmetics, resulting in a different scope of these products in the United States than in China. Currently, hand disinfection products, toothbrushes, dental floss, laser rangefinders, ultrasonic humidifiers and other radiation electronic products, as well as drugs and food ingredients that need to be further processed into finished products, are all under the jurisdiction of the US FDA. Click here to learn about FDA regulations and requirements for free. Therefore, companies must carry out necessary registration or filing before exporting to the United States. Many domestic companies have been refused entry by the FDA or even been added to the blacklist because they do not understand these.
It should be noted that registration is required, but it does not mean that the FDA has certified these products. Products currently certified and approved by the US FDA include new drugs, generic drugs and most Class III medical devices (such as artificial hearts).