FDA is the abbreviation of the Food and Drug Administration. It is one of the executive agencies established by the US government within the Department of Health and Human Services (DHHS) and the Department of Public Health (PHS).

FDA Certification Scope: 

The scope of the FDA regulatory agency is very broad. The responsibilities of the FDA are closely related to those of several other government agencies. Consumers often feel frustrated and confused, and are unsure of which appropriate regulatory agency to contact. The following is a list of traditional recognized product categories under the jurisdiction of the FDA; however, this is not an exhaustive list. Generally speaking, the FDA stipulates: 

Food

Dietary supplements 

Bottled water 

Food additives 

Infant formula milk powder 

Other foods (although the United States Department of Agriculture plays a leading role in regulating certain meats, poultry, and egg products) 

Cosmetics

Color additives in cosmetics and other personal care products 

Skin moisturizer and cleanser 

Nail polish and perfume 

Medication

Prescription drugs (all are brand names and generic names) 

Over-the-counter drugs (OTC drugs) 

Medical devices

Simple items, such as depression and bed covers 

Complex technologies, such as pacemakers for the heart 

Dental equipment 

Surgical implants and prosthetics 

Biological agents 

vaccine

Blood and blood products 

Cell and gene therapy products 

Organization and organizational products 

Allergen 

Electronics that emit radiation 

Microwave oven

X-ray equipment 

Laser products 

Ultrasound therapy equipment 

Mercury lamp 

Solar lamp 

Veterinary products 

Livestock feed 

Pet food 

Veterinary drugs and equipment 

Tobacco products 

Cigarettes

Cigarettes and tobacco 

The tobacco used by cigarettes 

Smokeless tobacco 

Our company mainly engages in the certification of electronic products that emit radiation in accordance with FDA standards. 

How to obtain FDA certification for radiation-emitting products 

Importers of radiation-emitting electronic products that comply with the FDA's implementation standards must submit a written statement regarding "Product Declaration for Radiation Control Standards" (FDA 2877) and other import information to the appropriate FDA Import Office through the U.S. Customs and Border Protection Agency (CBP). Electronic products that do not meet the applicable performance standards or do not have a certification label or label (21 CFR 1010.2) for each product are not allowed to enter. If your product complies with the performance standards, it indicates that you have reported your product to the FDA by including your registration number in the form of FDA 2877. 

2. When preparing the product report, make sure to identify your American agent.