# 21 C.F.R. § 814.126 (2026): Postapproval requirements and reports > Federal · Regulations · In force URL: https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_126 ## Section - **Citation:** 21 C.F.R. § 814.126 (2026) - **Heading:** Postapproval requirements and reports - **Jurisdiction:** Federal - **Kind:** Regulations - **Status:** In force - **Text as of:** August 14, 2026 - **Source:** Compiled text - **Location:** Title 21 CFR: Food and Drugs / Chapter I: FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES / Part 814: PREMARKET APPROVAL OF MEDICAL DEVICES / Subpart H: Humanitarian Use Devices / § 814.126: § 814.126 Postapproval requirements and reports. ## Text (a) An HDE approved under this subpart H shall be subject to the postapproval requirements and reports set forth under subpart E of this part, as applicable, with the exception of § 814.82(a)(7). In addition, medical device reports submitted to FDA in compliance with the requirements of part 803 of this chapter shall also be submitted to the IRB of record. (b) In addition to the reports identified in paragraph (a) of this section, the holder of an approved HDE shall prepare and submit the following complete, accurate, and timely reports: (1) Periodic reports. An HDE applicant is required to submit reports in accordance with the approval order. Unless FDA specifies otherwise, any periodic report shall include: (i) An update of the information required under § 814.102(a) in a separately bound volume; (ii) An update of the information required under § 814.104(b)(2), (b)(3), and (b)(5); (iii) The number of devices that have been shipped or sold since initial marketing approval under this subpart H and, if the number shipped or sold exceeds 8,000, an explanation and estimate of the number of devices used per patient. If a single device is used on multiple patients, the applicant shall submit an estimate of the number of patients treated or diagnosed using the device together with an explanation of the basis for the estimate; (iv) Information describing the applicant's clinical experience with the device since the HDE was initially approved. This information shall include safety information that is known or reasonably should be known to the applicant, medical device reports made under part 803 of this chapter, any data generated from the postmarketing studies, and information (whether published or unpublished) that is known or reasonably expected to be known by the applicant that may affect an evaluation of the safety of the device or that may affect the statement of contraindications, warnings, precautions, and adverse reactions in the device's labeling; and reports made under part 803 of this chapter, any data generated from the postmarketing studies, and information (whether published or unpublished) that is known or reasonably expected to be known by the applicant that may affect an evaluation of the safety of the device or that may affect the statement of contraindications, warnings, precautions, and adverse reactions in the device's labeling; and (v) A summary of any changes made to the device in accordance with supplements submitted under § 814.108. If information provided in the periodic reports, or any other information in the possession of FDA, gives the agency reason to believe that a device raises public health concerns or that the criteria for exemption are no longer met, the agency may require the HDE holder to submit additional information to demonstrate continued compliance with the HDE requirements. (2) Other. An HDE holder shall maintain records of the names and addresses of the facilities to which the HUD has been shipped, correspondence with reviewing IRB's, as well as any other information requested by a reviewing IRB or FDA. Such records shall be maintained in accordance with the HDE approval order. [61 FR 33244, June 26, 1996, as amended at 63 FR 59221, Nov. 3, 1998; 71 FR 16228, Mar. 31, 2006; 82 FR 26349, June 7, 2017] ## Nearby sections - [21 C.F.R. § 814.100 (2026) § 814.100 Purpose and scope.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_100.md) - [21 C.F.R. § 814.102 (2026) § 814.102 Designation of HUD status.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_102.md) - [21 C.F.R. § 814.104 (2026) § 814.104 Original applications.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_104.md) - [21 C.F.R. § 814.106 (2026) § 814.106 HDE amendments and resubmitted HDE's.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_106.md) - [21 C.F.R. § 814.108 (2026) § 814.108 Supplemental applications.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_108.md) - [21 C.F.R. § 814.110 (2026) § 814.110 New indications for use.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_110.md) - [21 C.F.R. § 814.112 (2026) § 814.112 Filing an HDE.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_112.md) - [21 C.F.R. § 814.114 (2026) § 814.114 Timeframes for reviewing an HDE.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_114.md) - [21 C.F.R. § 814.116 (2026) § 814.116 Procedures for review of an HDE.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_116.md) - [21 C.F.R. § 814.118 (2026) § 814.118 Denial of approval or withdrawal of approval of an HDE.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_118.md) - [21 C.F.R. § 814.120 (2026) § 814.120 Temporary suspension of approval of an HDE.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_120.md) - [21 C.F.R. § 814.122 (2026) § 814.122 Confidentiality of data and information.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_122.md) - [21 C.F.R. § 814.124 (2026) § 814.124 Institutional Review Board requirements.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_124.md) - [21 C.F.R. § 814.126 (2026) § 814.126 Postapproval requirements and reports.](https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_126.md) --- Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/CFR_T21_P814_S814_126. 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