{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\" and document_type = \"Rule\" sorted by posted_date descending", "rows": [["FDA-2026-N-4274-0001", "FDA", "FDA-2026-N-4274", "Medical Devices; Immunology and Microbiology Devices; Classification of the Device To Detect and Identify Microorganism Nucleic Acids and Resistance Markers From Patients With Suspected Orthopedic Infection", "Rule", "Final Rule", "2026-05-12T04:00:00Z", 2026, 5, null, null, "2026-05-12T22:59:34Z", "2026-09335", 0, 0, "09000064b92d17ac"], ["FDA-2026-N-4659-0001", "FDA", "FDA-2026-N-4659", "Medical Devices; Obstetrical and Gynecological Devices; Classification of the External Condom for Anal Intercourse or Vaginal Intercourse", "Rule", "Final Rule", "2026-05-08T04:00:00Z", 2026, 5, null, null, "2026-05-08T17:10:31Z", "2026-09152", 0, 0, "09000064b92c973f"], ["FDA-2026-N-4644-0001", "FDA", "FDA-2026-N-4644", "Medical Devices; Immunology and Microbiology Devices; Classification of the Device To Preserve and Stabilize Relative Abundances of Microbial Nucleic Acids in Clinical Samples", "Rule", "Final Rule", "2026-05-06T04:00:00Z", 2026, 5, "2026-05-06T04:00:00Z", null, "2026-05-06T17:36:42Z", "2026-08811", 0, 0, "09000064b92c6542"], ["FDA-2026-N-4643-0001", "FDA", "FDA-2026-N-4643", "Medical Devices; Immunology and Microbiology Devices; Classification of the Circulating Tumor Cell Enrichment Device", "Rule", "Final Rule", "2026-05-06T04:00:00Z", 2026, 5, "2026-05-06T04:00:00Z", null, "2026-05-06T17:30:07Z", "2026-08812", 0, 0, "09000064b92c6687"], ["FDA-2026-N-4645-0001", "FDA", "FDA-2026-N-4645", "Medical Devices; Ophthalmic Devices; Classification of the Corneal Storage Medium With Preservatives Including Antifungals", "Rule", "Final Rule", "2026-05-06T04:00:00Z", 2026, 5, "2026-05-06T04:00:00Z", null, "2026-05-06T17:43:01Z", "2026-08813", 0, 0, "09000064b92c5b59"], ["FDA-2026-N-4273-0001", "FDA", "FDA-2026-N-4273", "Medical Devices; General and Plastic Surgery Devices; Classification of the Phototherapy Device for Reducing the\nAppearance of Acute Post-Surgical Incisions", "Rule", "Final Rule", "2026-05-01T04:00:00Z", 2026, 5, "2026-05-01T04:00:00Z", null, "2026-05-01T17:52:35Z", "2026-08497", 0, 0, "09000064b92bb721"], ["FDA-2026-N-4269-0001", "FDA", "FDA-2026-N-4269", "Medical Devices; Neurological Devices; Classification of the Brain Temperature Measurement System", "Rule", "Final Rule", "2026-04-30T04:00:00Z", 2026, 4, null, null, "2026-04-30T18:05:38Z", "2026-08425", 0, 0, "09000064b92b7ed2"], ["FDA-2026-N-3946-0001", "FDA", "FDA-2026-N-3946", "Medical Devices; Cardiovascular Devices; Classification of the Laser-Powered Inferior Vena Cava Filter Retrieval Catheter", "Rule", "Final Rule", "2026-04-30T04:00:00Z", 2026, 4, null, null, "2026-04-30T17:49:39Z", "2026-08426", 0, 0, "09000064b92b8047"], ["FDA-2026-N-4270-0001", "FDA", "FDA-2026-N-4270", "Medical Devices; Radiology Devices; Classification of the Radiation Therapy Marking Device", "Rule", "Final Rule", "2026-04-30T04:00:00Z", 2026, 4, null, null, "2026-04-30T18:00:48Z", "2026-08424", 0, 0, "09000064b92b7f21"], ["FDA-2026-N-3900-0001", "FDA", "FDA-2026-N-3900", "Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Setmelanotide Eligibility Gene Variant Detection System", "Rule", "Final Rule", "2026-04-22T04:00:00Z", 2026, 4, null, null, "2026-04-22T16:47:09Z", "2026-07863", 0, 0, "09000064b929ebd0"], ["FDA-2026-N-3930-0001", "FDA", "FDA-2026-N-3930", "Medical Devices; Immunology and Microbiology Devices; Classification of the Alzheimer\u2019s Disease Pathology Assessment Test", "Rule", "Final Rule", "2026-04-22T04:00:00Z", 2026, 4, null, null, "2026-04-22T17:00:14Z", "2026-07860", 0, 0, "09000064b929eb70"], ["FDA-2026-N-3929-0001", "FDA", "FDA-2026-N-3929", "Medical Devices; Anesthesiology Devices; Classification of the Device for Sleep Apnea Testing Based on Mandibular Movement", "Rule", "Final Rule", "2026-04-22T04:00:00Z", 2026, 4, null, null, "2026-04-22T16:51:45Z", "2026-07862", 0, 0, "09000064b929ebcb"], ["FDA-2026-N-3928-0001", "FDA", "FDA-2026-N-3928", "Medical Devices; Ophthalmic Devices; Classification of the Digital Therapy Device for Amblyopia", "Rule", "Final Rule", "2026-04-22T04:00:00Z", 2026, 4, null, null, "2026-04-22T22:55:05Z", "2026-07861", 0, 0, "09000064b929eb71"], ["FDA-2020-N-1053-0041", "FDA", "FDA-2020-N-1053", "Physical Medicine Devices; Reclassification of Non-Invasive Bone Growth Stimulators", "Rule", "Final Rule", "2026-04-16T04:00:00Z", 2026, 4, null, null, "2026-04-16T18:27:17Z", "2026-07366", 0, 0, "09000064b928652b"], ["FDA-2026-N-2887-0001", "FDA", "FDA-2026-N-2887", "Medical Devices; Orthopedic Devices; Classification of the Manual Surgical Instrument for Appropriate Patient Selection for Orthopedic Implant", "Rule", "Final Rule", "2026-04-16T04:00:00Z", 2026, 4, null, null, "2026-04-16T18:01:43Z", "2026-07367", 0, 0, "09000064b92866e8"], ["FDA-2025-N-0002-0005", "FDA", "FDA-2025-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug Application; Change of Sponsor; Change of Sponsor Address", "Rule", "Final Rule", "2026-04-16T04:00:00Z", 2026, 4, null, null, "2026-04-16T18:09:43Z", "2026-07500", 0, 0, "09000064b928669d"], ["FDA-2026-N-2959-0001", "FDA", "FDA-2026-N-2959", "Medical Devices; Ear, Nose, and Throat Devices; Classification of the Transcutaneous Electrical Nerve Stimulator for the Relief of Congestion", "Rule", "Final Rule", "2026-04-16T04:00:00Z", 2026, 4, null, null, "2026-04-16T18:13:32Z", "2026-07365", 0, 0, "09000064b9286697"], ["FDA-2022-N-0794-0021", "FDA", "FDA-2022-N-0794", "General and Plastic Surgery Devices; Reclassification of Optical Diagnostic Devices for Melanoma Detection and Electrical Impedance Spectrometers,\nTo Be Renamed Software-Aided Adjunctive Diagnostic Devices for Use on Skin Lesions by Physicians Trained in the Diagnosis and Management of\nSkin Cancer", "Rule", "Final Rule", "2026-03-25T04:00:00Z", 2026, 3, null, null, "2026-03-25T23:46:39Z", "2026-05772", 0, 0, "09000064b9235032"], ["FDA-2024-C-3384-0014", "FDA", "FDA-2024-C-3384", "Listing of Color Additive Exempt From Certification; Spirulina Extract; Delay of Effective Date", "Rule", "Delay of Effective Date", "2026-03-24T04:00:00Z", 2026, 3, "2026-03-24T04:00:00Z", null, "2026-03-24T18:46:35Z", "2026\u201305733", 0, 0, "09000064b922fb68"], ["FDA-2024-C-3384-0015", "FDA", "FDA-2024-C-3384", "Listing of Color Additive Exempt From Certification; Spirulina Extract; Delay of Effective Date", "Rule", "Final Rule", "2026-03-24T04:00:00Z", 2026, 3, "2026-03-24T04:00:00Z", null, "2026-03-27T17:28:03Z", "2026-05733", 0, 0, "09000064b9231509"], ["FDA-2024-C-1085-0214", "FDA", "FDA-2024-C-1085", "Listing of Color Additive Exempt From Certification; Beetroot Red; Delay of Effective Date", "Rule", "Delay of Effective Date", "2026-03-24T04:00:00Z", 2026, 3, null, null, "2026-03-24T21:01:53Z", "2026-05732", 0, 0, "09000064b922fb4f"], ["FDA-2021-N-1351-0056", "FDA", "FDA-2021-N-1351", "Revising the National Drug Code Format and Drug Label Barcode Requirements", "Rule", "Final Rule", "2026-03-05T05:00:00Z", 2026, 3, "2026-03-05T05:00:00Z", null, "2026-03-05T19:38:29Z", "2026-04368", 0, 0, "09000064b91f375e"], ["FDA-2024-N-4016-0010", "FDA", "FDA-2024-N-4016", "Revocation of Regulations Regarding the Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and the European Community", "Rule", "Final Rule", "2026-02-19T05:00:00Z", 2026, 2, "2026-02-19T05:00:00Z", null, "2026-02-19T20:44:43Z", "2026-03286", 0, 0, "09000064b91bd3cf"], ["FDA-2020-N-1383-0042", "FDA", "FDA-2020-N-1383", "Revocation of Methods of Analysis Regulation", "Rule", "Final Rule", "2026-02-19T05:00:00Z", 2026, 2, "2026-02-19T05:00:00Z", null, "2026-02-19T20:49:20Z", "2026-03285", 0, 0, "09000064b91bd38a"], ["FDA-2024-C-3384-0003", "FDA", "FDA-2024-C-3384", "Listing of Color Additives Exempt From Certification; Spirulina Extract", "Rule", "Final Rule", "2026-02-06T05:00:00Z", 2026, 2, "2026-02-06T05:00:00Z", "2026-03-10T03:59:59Z", "2026-03-09T09:00:25Z", "2026-02314", 0, 0, "09000064b9195bcf"], ["FDA-2025-N-0002-0004", "FDA", "FDA-2025-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug\nApplication; Change of Sponsor; Change of Sponsor Address", "Rule", "Final Rule", "2026-02-06T05:00:00Z", 2026, 2, "2026-02-06T05:00:00Z", null, "2026-02-06T20:40:05Z", "2026-02331", 0, 0, "09000064b9195a5c"], ["FDA-2024-C-1085-0003", "FDA", "FDA-2024-C-1085", "Listing of Color Additives Exempt From Certification; Beetroot Red", "Rule", "Final Rule", "2026-02-06T05:00:00Z", 2026, 2, "2026-02-06T05:00:00Z", "2026-03-10T03:59:59Z", "2026-03-10T09:00:09Z", "2026-02313", 0, 0, "09000064b91929e7"], ["FDA-2025-N-6025-0001", "FDA", "FDA-2025-N-6025", "Medical Devices; Neurological Devices; Classification of the Electrical Tongue Nerve Stimulator To Treat Motor Deficits", "Rule", "Final Rule", "2025-12-19T05:00:00Z", 2025, 12, "2025-12-19T05:00:00Z", null, "2025-12-19T21:24:58Z", "2025-23413", 0, 0, "09000064b90eed4c"], ["FDA-2025-N-4635-0001", "FDA", "FDA-2025-N-4635", "Medical Devices; Quality Management System Regulation Technical Amendments", "Rule", "Final Rule", "2025-12-04T05:00:00Z", 2025, 12, "2025-12-04T05:00:00Z", null, "2025-12-04T20:51:36Z", "2025-21955", 0, 0, "09000064b90addd8"], ["FDA-2025-N-4680-0001", "FDA", "FDA-2025-N-4680", "Medical Devices; Neurological Devices; Classification of Field Generator Positioning Device", "Rule", "Final Rule", "2025-11-26T05:00:00Z", 2025, 11, null, null, "2025-11-26T19:18:25Z", "2025-21218", 0, 0, "09000064b909eb80"], ["FDA-2025-N-4645-0001", "FDA", "FDA-2025-N-4645", "Medical Devices; Gastroenterology-Urology Devices; Classification of the Anchored Esophageal Sheath", "Rule", "Final Rule", "2025-11-26T05:00:00Z", 2025, 11, null, null, "2025-11-26T19:27:15Z", "2025-21217", 0, 0, "09000064b9099738"], ["FDA-2021-C-0522-0008", "FDA", "FDA-2021-C-0522", "Listing of Color Additives Exempt From Certification; Gardenia (Genipin) Blue; Confirmation of Effective Date", "Rule", "Confirmation of Effective Date", "2025-10-01T04:00:00Z", 2025, 10, "2025-10-01T04:00:00Z", null, "2025-10-01T16:19:10Z", "2025-19166", 0, 0, "09000064b8feca5c"], ["FDA-2025-N-1184-0013", "FDA", "FDA-2025-N-1184", "Revocation of Food Standards for 11 Products Not Currently Sold; Confirmation of Effective Date", "Rule", "Direct Final Rule", "2025-09-26T04:00:00Z", 2025, 9, "2025-09-26T04:00:00Z", null, "2025-09-26T20:06:47Z", "2025-18730", 0, 0, "09000064b8fdf0a2"], ["FDA-2011-N-0179-0040", "FDA", "FDA-2011-N-0179", "Prior Notice: Adding Requirement To Submit Mail Tracking Number for Articles of Food Arriving by International Mail and Timeframe for Post-Refusal and Post-Hold Submissions", "Rule", "Final Rule", "2025-09-25T04:00:00Z", 2025, 9, null, null, "2025-09-25T18:43:29Z", "2025-18655", 0, 0, "09000064b8fdc155"], ["FDA-2025-N-0002-0003", "FDA", "FDA-2025-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug Applications; Change of Sponsor; Change of Sponsor Address; Correction", "Rule", "Correction", "2025-09-19T04:00:00Z", 2025, 9, "2025-09-19T04:00:00Z", null, "2025-09-19T18:10:54Z", "2025-18217", 0, 0, "09000064b8fba369"], ["FDA-2025-N-1730-0001", "FDA", "FDA-2025-N-1730", "Regulation Identification Number 0910\u2013AJ05 Medical Devices; Laboratory Developed Tests; Implementation of Vacatur", "Rule", "Final Rule", "2025-09-19T04:00:00Z", 2025, 9, "2025-09-19T04:00:00Z", null, "2025-09-19T18:14:38Z", "2025-18239", 0, 0, "09000064b8fb1036"], ["FDA-2018-N-3303-0024", "FDA", "FDA-2018-N-3303", "Radiological Health Regulations; Technical Amendments", "Rule", "Final Rule", "2025-09-18T04:00:00Z", 2025, 9, "2025-09-18T04:00:00Z", null, "2025-09-18T18:59:50Z", "2025-18080", 0, 0, "09000064b8fb0f97"], ["FDA-2024-N-3533-0032", "FDA", "FDA-2024-N-3533", "Microbiology Devices; Reclassification of Antigen, Antibody, and Nucleic Acid-Based Hepatitis B Virus Assay Devices", "Rule", "Final Rule", "2025-09-18T04:00:00Z", 2025, 9, "2025-09-18T04:00:00Z", null, "2025-09-18T18:53:51Z", "2025-18082", 0, 0, "09000064b8fb1032"], ["FDA-2021-F-0366-0002", "FDA", "FDA-2021-F-0366", "Food Additives Permitted for Direct Addition to Food for Human Consumption; Vitamin D3 in Yogurt and Other Cultured Dairy Products Fermented With Lactobacillus delbrueckii, Subspecies bulgaricus, and Streptococcus thermophilus", "Rule", "Final Rule", "2025-09-04T04:00:00Z", 2025, 9, "2025-09-04T04:00:00Z", "2025-10-07T03:59:59Z", "2025-10-07T01:16:03Z", "2025-16946", 0, 0, "09000064b8f40d02"], ["FDA-2022-F-2725-0008", "FDA", "FDA-2022-F-2725", "Secondary Direct Food Additives Permitted in Food for Human Consumption; Hydrogen Peroxide", "Rule", "Final Rule", "2025-09-03T04:00:00Z", 2025, 9, "2025-09-03T04:00:00Z", "2025-10-04T03:59:59Z", "2025-10-07T01:16:03Z", "2025-16898", 0, 0, "09000064b8f38e11"], ["FDA-2025-N-2427-0001", "FDA", "FDA-2025-N-2427", "Advisory Committee; Arthritis Advisory Committee; Termination; Removal From List of Standing Committees", "Rule", "Final Rule", "2025-08-29T04:00:00Z", 2025, 8, null, null, "2025-08-29T17:17:40Z", "2025-16629", 0, 0, "09000064b8f25fe7"], ["FDA-2025-N-0002-0002", "FDA", "FDA-2025-N-0002", "New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug\nApplications; Change of Sponsor; Change of Sponsor Address", "Rule", "Final Rule", "2025-08-22T04:00:00Z", 2025, 8, "2025-08-22T04:00:00Z", null, "2025-08-22T17:34:47Z", "2025-16079", 0, 0, "09000064b8f0b41a"], ["FDA-2025-N-2107-0001", "FDA", "FDA-2025-N-2107", "Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Menopause Test System", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:51:06Z", "2025-16036", 0, 0, "09000064b8f0b22d"], ["FDA-2025-N-2106-0001", "FDA", "FDA-2025-N-2106", "Medical Devices; Immunology and Microbiology Devices; Classification of the Device That Detects Nucleic Acid Sequences From Microorganisms Associated With Vaginitis and Bacterial Vaginosis", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:03:43Z", "2025-16030", 0, 0, "09000064b8f0b385"], ["FDA-2025-N-2520-0001", "FDA", "FDA-2025-N-2520", "Medical Devices; Orthopedic Devices; Classification of Orthopedic Manual Surgical Instrumentation for Use With Total Disc Replacement Devices", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:08:45Z", "2025-16039", 0, 0, "09000064b8f0b382"], ["FDA-2025-N-2788-0001", "FDA", "FDA-2025-N-2788", "Medical Devices; Immunology and Microbiology Devices; Classification of A Multiplex Respiratory Panel To Detect and Identify Emerging Respiratory Pathogen(s) and Common Respiratory Pathogens in Human Clinical Specimens", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:33:55Z", "2025-16034", 0, 0, "09000064b8f0b2f1"], ["FDA-2024-C-0971-0009", "FDA", "FDA-2024-C-0971", "Listing of Color Additives Exempt From Certification; Butterfly Pea Flower Extract; Confirmation of Effective Date", "Rule", "Confirmation of Effective Date", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:22:33Z", "2025-16045", 0, 0, "09000064b8f0b33c"], ["FDA-2025-N-2523-0001", "FDA", "FDA-2025-N-2523", "Medical Devices; Orthopedic Devices; Classification of Orthopedic Manual Surgical Instrumentation for Use With Non-Fusion Spinous Process Spacer Devices", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:41:21Z", "2025-16040", 0, 0, "09000064b8f0b2b9"], ["FDA-2023-C-0544-0010", "FDA", "FDA-2023-C-0544", "Listing of Color Additives Exempt From Certification; Calcium Phosphate; Confirmation of Effective Date", "Rule", "Confirmation of Effective Date", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:30:28Z", "2025-16047", 0, 0, "09000064b8f0b2f5"], ["FDA-2021-C-0925-0007", "FDA", "FDA-2021-C-0925", "Listing of Color Additives Exempt From Certification; Galdieria Extract Blue; Confirmation of Effective Date", "Rule", "Confirmation of Effective Date", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T16:53:21Z", "2025-16046", 0, 0, "09000064b8f0b3ce"], ["FDA-2025-N-2369-0001", "FDA", "FDA-2025-N-2369", "Medical Devices; Radiology Devices; Classification of the Liver Iron Concentration Imaging Companion Diagnostic for Deferasirox", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T16:47:29Z", "2025-16033", 0, 0, "09000064b8f0b3d1"], ["FDA-2025-N-2219-0001", "FDA", "FDA-2025-N-2219", "Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Pharmacogenetic Assessment System", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:13:17Z", "2025-16037", 0, 0, "09000064b8f0b340"], ["FDA-2025-N-2108-0001", "FDA", "FDA-2025-N-2108", "Medical Devices; Immunology and Microbiology Devices; Classification of the Anti-Phospholipase A2 Receptor Immunological Test System", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T16:57:13Z", "2025-16031", 0, 0, "09000064b8f0b386"], ["FDA-2025-N-2424-0001", "FDA", "FDA-2025-N-2424", "Medical Devices; Immunology and Microbiology Devices; Classification of the Mutation Detection Test for Myeloproliferative Neoplasms", "Rule", "Final Rule", "2025-08-21T04:00:00Z", 2025, 8, null, null, "2025-08-21T17:44:12Z", "2025-16038", 0, 0, "09000064b8f0b275"], ["FDA-2025-N-2110-0001", "FDA", "FDA-2025-N-2110", 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