FDA approvals

FDA approvals are official confirmations that a medical product—like a drug, device, or treatment—is safe and effective for public use. The process involves rigorous testing, clinical trials, and data review to ensure benefits outweigh risks. Once approved, the product can be marketed and prescribed, but ongoing monitoring continues for safety. Approval levels vary depending on the product and intended use, ensuring that healthcare providers and consumers have confidence in the safety and efficacy of new medical solutions.