Post-market surveillance

Post-market surveillance is the ongoing FDA monitoring of devices after clearance, driven by adverse event reports (MAUDE), recall records, and registration data.

Three of the datasets touching this slice - MAUDE, the Device Recalls API, and the Registration & Listing API - each cover one leg of that monitoring.

In this catalog it appears concretely: - tags (MAUDE): post-market-surveillance, device-safety. - tags (related): openFDA Device Recalls API serves the same surveillance workflow.

Conventions decide whether two sources can be joined at all. Buy one side of an analysis that ignores this convention and every reconciliation step — calendar alignment, unit conversion, entity matching — lands on your team instead of the vendor's.

The failure mode is concrete: the label appears in a listing, the delivered files tell a different story, and the gap surfaces mid-project when fixing it is most expensive.

You rarely have to take a vendor's word for it. 82.4% of the 1,744 datasets Datadory catalogs are free to access, and tags (MAUDE): post-market-surveillance, device-safety lets you inspect the real artifact before any budget is committed.

Treat every claim of this attribute as testable:

1. Open tags (MAUDE): post-market-surveillance, device-safety and compare its listing against the delivered artifact before paying for a commercial equivalent.
2. Open tags (related): openFDA Device Recalls API serves the same surveillance workflow and compare its listing against the delivered artifact before paying for a commercial equivalent.
3. Pin down update cadence in writing. Across this catalog, 22.6% of 1,744 datasets refresh daily and 64 still arrive only through a manual request form, so ask exactly how fresh each release is.
4. Check whether definitions are verified at all. Field definitions are verified for 1495 of 1,744 datasets (85.7%), and any source you license should meet that bar.
5. Price the delivery route before the license. In this catalog bulk download is the most common access method (725 datasets) ahead of official APIs (574), and 379 sources still require scraping — a maintenance cost that lands on you, not the vendor.

See the term applied to real records: health-care-equipment data, health-care-supplies data.

Adjacent concepts worth reading next: - device recall - Establishment registration - MAUDE - Medical Device Report (MDR)