Which regulatory body oversees the safe handling and reprocessing of medical devices in the United States?

The Food and Drug Administration (FDA) is the regulatory body responsible for overseeing the safe handling and reprocessing of medical devices in the United States. The FDA establishes guidelines and regulations to ensure that medical devices are safe for patients and are manufactured and processed in compliance with required standards. This includes comprehensive oversight of device labeling, manufacturing processes, and post-market surveillance, making the FDA crucial in maintaining public health safety.

The other organizations mentioned serve important roles within the healthcare system but do not focus exclusively on medical device regulation. The American Medical Association (AMA) primarily advocates for physicians and medical professionals, while the Centers for Disease Control and Prevention (CDC) focuses on public health and disease prevention. The National Institutes of Health (NIH) is involved in medical research and funding studies but does not regulate medical device safety. Thus, the FDA is uniquely positioned with the authority to establish and enforce regulations governing medical devices.