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# Medical Device Reporting Info Collection
- URL: https://www.fdaweb.com/medical-device-reporting-info-collection/
- Published: 2021-04-29T12:00:00.000Z
- Updated: 2026-09-14T16:56:58.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5149220

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “Medical Device Reporting — 21 CFR Part 803” (OMB Control Number 0910**\-**0437). The collection supports FDA regulations and its Medical Device Reporting program that require user facilities, manufacturers, importers, and distributors of medical devices to report adverse events involving medical devices to FDA. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2021-04-29/pdf/2021-08962.pdf?ref=fdaweb.com).