Final rule 2025-21955
Medical Devices; Quality Management System Regulation Technical Amendments
The Food and Drug Administration (FDA, the Agency, or we) is amending certain medical device regulations to revise references and language in existing Code of Federal Regulations (CFR) provisions to conform with the final rule "Medical Devices; Quality System Regulation Amendments" (QMSR Final Rule). This rule does not impose any new requirements on affected parties. This action is editorial in nature to correct errors, conform regulatory references, and ensure accuracy and clarity in the Agency's regulations.
Source-supplied record
Document details
- Document number
- 2025-21955
- Published
- Dec 4, 2025
- Effective
- Feb 2, 2026
- Comments close
- Not supplied
- Federal Register citation
- 90 FR 55978
Docket identifiers
- Docket No. FDA-2025-N-4635
CFR references
- Title 21, part 801
- Title 21, part 803
- Title 21, part 812
- Title 21, part 860
- Title 21, part 862
- Title 21, part 864
- Title 21, part 866
- Title 21, part 868
- Title 21, part 872
- Title 21, part 874
- Title 21, part 876
- Title 21, part 878
- Title 21, part 880
- Title 21, part 882
- Title 21, part 886
- Title 21, part 888
- Title 21, part 890
- Title 21, part 892