The FDA UDI compliance is a publicly accessible database that contains key information about each medical device with a UDI. The UDI is a unique code assigned to medical devices that allows for unambiguous identification and traceability throughout the supply chain. By implementing UDIs, the FDA aims to enhance patient safety, streamline recalls, and facilitate post-market surveillance. https://fdalisting.com/page/104/us-fda-global-device-identification-gudid-unique-device-identifiers-udi/