FDA Approval is the process by which the U.S. Food and Drug Administration evaluates and authorizes new drugs, medical devices, and other products for public use. This process ensures that these products are safe and effective for their intended purposes. Companies must submit extensive data from clinical trials to demonstrate their product's safety and efficacy. Once the FDA reviews the submitted data, it may grant approval, allowing the product to be marketed and sold in the United States. This approval is crucial for protecting public health and ensuring that consumers have access to reliable and effective medical treatments.