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# Info Collection on Device Registration/Listing
- URL: https://www.fdaweb.com/info-collection-on-device-registration-listing-2/
- Published: 2022-06-23T12:00:00.000Z
- Updated: 2026-09-14T17:49:41.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5152141

*Federal Register* notice: FDA has submitted to OMB an information collection extension entitled “Establishment Registration and Device Listing for Manufacturers and Importers of Devices — 21 CFR Part 807, Subparts A Through D” (OMB Control Number 0910-0625). The collection supports agency regulations that require medical device establishment owners and operators electronically submit establishment registration and device listing information. To view the notice, click [here](https://public-inspection.federalregister.gov/2022-13522.pdf?ref=fdaweb.com).