China and the United States have different definitions of food, medicine, medical devices, radiation electronic products and cosmetics, which leads to different application scopes of these products in the United States and China. At present, disinfection products, toothbrush, dental floss, laser rangefinder, ultrasonic humidifier and other radiation electronic products, as well as medicines and food ingredients that need to be further processed into finished products, are all under the jurisdiction of the US FDA. Therefore, enterprises must register or put on record before exporting to the United States. Many domestic enterprises have been refused entry by the FDA and even blacklisted because they don't understand this.
It should be noted that registration is necessary, but it does not mean that the FDA has certified these products. At present, products certified and approved by FDA include new drugs, generic drugs and most of the three types of medical devices (such as artificial hearts).
Supplementary science: what is FDA certification?
The FDA is the abbreviation of the US Food and Drug Administration, namely the US Food and Drug Administration. Accurately speaking, the US FDA does not certify most products, but enterprises must file or register, otherwise, the US FDA has the right to take actions against goods, including detaining goods, refusing entry or even destroying them, blacklisting enterprises, and so on. The products under the jurisdiction of FDA include food, food contact materials, medicines, pharmaceutical ingredients, cosmetics, medical devices, radiation electronic products and tobacco products. Before entering the United States, enterprises need to make necessary registration. For more information about FDA certification, please contact our company #Registrar Corp#