Certification introduction:

FDA (Food and Drug Administration) certification is a food or drug certificate of conformity issued by the U.S. Food and Drug Administration. Due to its scientific nature and rigor, this certification has become a recognized standard around the world. FDA-approved drugs can be sold not only in the United States, but also in most countries and regions around the world. FDA is the abbreviation of the United States Food and Drug Administration. It is an international medical review authority authorized by the U.S. Congress and the federal government. It is the highest law enforcement agency specializing in food and drug administration.

The FDA is a government health supervision agency composed of professionals such as doctors, lawyers, microbiologists, pharmacologists, chemists and statisticians, and is committed to protecting, promoting and enhancing national health. Food, drugs, cosmetics and medical devices certified by the FDA are safe and effective for the human body. In nearly 100 countries including the United States, only FDA-approved materials, equipment and technologies can be used for commercial clinical applications.

FDA classification:

1.FDA testing of food raw materials

Food Contact Materials (FCM) refers to materials that come into contact with food during normal use of the product. Because it is in direct contact with food, it is called the "underwear" of food. Its safety directly affects food safety and is also the most critical control point for enterprises. Products involved in food contact materials include food packaging, tableware, kitchen utensils, food processing machinery and kitchen utensils, etc. Food contact materials include: plastics, resins, rubber, silicone, metals, alloys, electroplating, paper, cardboard, glass, ceramics, enamel, colorants, printing coatings, inks, etc.

Food contact materials and products may affect the smell, taste and color of food during the process of contact with food, and may release a certain amount of toxic chemical components such as heavy metals and toxic additives. These chemicals can migrate into food. Ingested by human body, harmful to human health.

2. Food FDA testing

3. Medical device FDA testing

4. Cosmetics FDA testing

5.FDA testing of drugs and biological products

The difference between FDA certification, FDA testing and FDA registration:

• It can be understood that FDA testing generally targets these types of products: 1. Class II and Class III medical devices; 2. Cosmetics and daily necessities; 3. Food contact materials;

• FDA registration is generally divided into: 1. Cosmetics; 2. LED and laser products; 3. Medical devices; 4. Food; 5. Drugs;

• FDA certification is the general term for FDA testing and FDA registration. Both can be called FDA certification. FDA certification is just a popular term.