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# Info Collection on MedSun Device Reporting
- URL: https://www.fdaweb.com/info-collection-on-medsun-device-reporting/
- Published: 2023-06-12T12:00:00.000Z
- Updated: 2026-09-14T18:38:32.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5154665

*Federal Register* notice: FDA has submitted to OMB an information collection extension entitled “Adverse Event Program for Medical Devices (Medical Product Safety Network (MedSun)). The collection supports FDA regulation requiring manufacturers and user facilities to report medical device-related deaths, serious injuries, and malfunctions. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2023-06-12/pdf/2023-12483.pdf?ref=fdaweb.com).