U.S. Rep. Scott A. Peters (D-California) is attempting to define “remanufacturing” when it comes to medical devices via H.R. 7253. The bill – “Clarifying Remanufacturing to Protect Patient Safety Act of 2022’’ – is co-sponsored by Rep. John Joyce (R-Pennsylvania) and Rep. Kim Schrier (D-Washington). “Remanufacturing” is a term that has befuddled healthcare technology management (HTM) professionals, original equipment manufacturers (OEMs), the FDA and other stakeholders for at least half a decade. H.R. 7253 appears to offer changes to 21 USC 360: Registration of producers of drugs or devices.