
The Food and Drug Administration (FDA)®
The Food and Drug Administration (FDA) prioritizes the protection of patient and consumer health. Its primary role is to safeguard public health by implementing and enforcing laws and regulations that ensure the safety, effectiveness, and security of human and animal drugs, biologics, medical devices, radiation-emitting products, cosmetics, and food items.
When a medical product (such as a drug, device, or biologic) is labeled as "FDA approved", it indicates that the FDA has thoroughly evaluated the product's safety and effectiveness. The approval signifies that the benefits of the product, both known and potential, outweigh any associated risks. Essentially, FDA approval means that the agency has concluded the product is safe and effective for its intended purpose.