How often must a device establishment registration be renewed?

Device establishment registration must be renewed annually to remain compliant with the requirements set by the FDA. This renewal process ensures that the agency has current information about the manufacturers, specifications, and activities of the establishments involved in medical device production. It is crucial for maintaining oversight and ensuring devices in the market meet regulatory standards. By requiring annual renewal, the FDA can effectively monitor changes in manufacturing practices, address potential safety issues, and facilitate communication regarding new devices and technologies. This systematic approach helps to safeguard public health by ensuring that only establishments that meet current regulatory criteria are permitted to manufacture and distribute medical devices.