Which organization regulates sterilization packaging material in the United States?

The Food and Drug Administration (FDA) is the organization responsible for regulating sterilization packaging materials in the United States. This is because the FDA oversees medical devices and materials that come into direct contact with healthcare procedures, ensuring they are safe, effective, and appropriately labeled. Sterilization packaging materials must meet specific standards to prevent contamination, maintain sterility, and ensure that they function as intended throughout the lifecycle of a medical device.

The other organizations mentioned have distinct roles: the Centers for Disease Control and Prevention (CDC) primarily focuses on infection control guidelines and public health recommendations but does not regulate packaging materials. The Environmental Protection Agency (EPA) is involved in environmental issues and substances that might affect environmental health but does not regulate sterilization packaging. The Occupational Safety and Health Administration (OSHA) establishes workplace safety standards primarily focused on protecting workers but does not regulate medical devices or their packaging. Thus, the FDA is the correct answer for this question regarding sterilization packaging materials.