What is the significance of the FDA in medical device regulation?

The role of the FDA in medical device regulation is fundamentally centered on ensuring that medical devices are safe and effective for public use. This mission is crucial because medical devices can have significant impacts on patient health and safety. The FDA evaluates evidence provided by manufacturers, which includes clinical data, before approving devices for market access. The agency also monitors devices post-approval through systems that track adverse events and device performance, ensuring ongoing compliance with safety standards. By prioritizing the safety and effectiveness of medical devices, the FDA ultimately protects public health and instills confidence in the medical technology used in healthcare settings.