Data source

Data from Data from U.S. Food and Drug Administration, delivered clean., delivered clean.

4 datasets pulled from Data from U.S. Food and Drug Administration, delivered clean.'s releases, checked field by field and shipped the way you want them — daily, weekly, or hourly, your call.

  • 4 datasets
  • 3 industrys
  • Real rows on request

Paper Plastic Packaging Products Materials

2
Paper Plastic Packaging Products Materials United States (federal regulatory scope under… · 2000-03-01/present

FDA Food Contact Notification (FCN) Inventory Data

Paper Plastic Packaging Products Materials EU-27 aggregate · 1997-2023

Eurostat Packaging Waste dataset (env_waspac) JSON API

Health Care Supplies

1
Health Care Supplies United States - devices regulated by the FDA… · Continuously maintained reference shelf

FDA Medical Devices Portal

Health Care Equipment

1
Health Care Equipment United States plus foreign reports involving… · Publicly releasable reports from roughly 1992…

openFDA Device Adverse Events (MAUDE) API

Pick a catch, see the rows.

Name any Data from U.S. Food and Drug Administration, delivered clean. dataset and we send real rows from it — not a screenshot of rows. 1,744 datasets. Pick your catch.

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Straight answers about Data from U.S. Food and Drug Administration, delivered clean. data

How many food contact notifications does Datadory deliver?

1,760 effective notifications at the July 2026 snapshot, continuous from March 2000 to present - the program's complete life. Each record names the substance, the notifier who filed it, the manufacturer or supplier it binds to, the intended use, the limitations and the effective date.

Does an FDA food contact notification apply to any company using the substance?

No. Under FD&C Act section 409(h)(2)(C), a notification is effective only for the manufacturer or supplier named in it. A competitor wanting the same substance for the same use files their own notification, which makes this a cleared chemical-plus-company register rather than an approved-additives whitelist.

What happens when one FDA notification replaces another?

Supersession lives in the table. The older row stays put carrying the replacing-notification number in its own column, so lineage resolves inside the data instead of across scattered announcements - and a historical pull stays interpretable between deliveries.

Can I get part of an FDA dataset as a sample first?

Yes, and we recommend it. Name the substance classes, notifiers or intended uses you care about on the food-contact side, or the device databases and sections you want mapped on the other, and the sample arrives cut that way - keyed identically to the recurring delivery, so validation becomes production without re-mapping.