HR 2372
Device act of 2025
Jurisdiction
US Congress
Session
119th Congress (2025-2026)
Last updated at
Jun 14, 2026, 6:50 AM
Take action
Sign in to record your position, submit testimony, or contact your legislator.
Sign in to take action- Introduced
- Passed House
- Passed Senate
- To President
- Became Law
Bill overview
The Device Act of 2025 aims to improve the regulation of medical devices by requiring manufacturers to report changes to device design and reprocessing instructions to the Food and Drug Administration (FDA). It also mandates notification to the FDA before making changes to how devices are communicated to foreign healthcare providers and establishes requirements for rapid assessment tests used to ensure the proper cleaning and sterilization of reusable devices. This legislation seeks to enhance device safety and efficacy through increased transparency and oversight.
Arguments in favor
Reasons to support this legislation.
No arguments in favor have been submitted.
Submit yoursArguments opposed
Reasons to oppose this legislation.
No arguments opposed have been submitted.
Submit yoursRead the latest version inline or switch to a previous version.