The purpose of the DEVICE Act of 2025 is to improve the safety and communication regarding medical devices. It aims to ensure that manufacturers provide timely information about changes to device designs and reprocessing instructions, and to enhance the cleanliness and effectiveness of reusable medical devices. Key provisions of the Act include new reporting requirements for manufacturers. They must notify the Secretary of Health and Human Services before making any changes to the design or reprocessing instructions of a medical device.