openFDA Device Enforcement Snapshot — ZentraFoundry

Collect public US openFDA device-enforcement product metadata through Apify.

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What does openFDA Device Enforcement Snapshot — ZentraFoundry do?

ZentraFoundry’s openFDA Device Enforcement Snapshot Actor collects publicly available US device-enforcement metadata. The current public Store example shows ten rows and names Power-Trialysis catheter references 5605150 and 5605200. An independent official openFDA lookup contains these references in Z-2984-2026, reported September 23, 2026. The configured latest-record endpoint currently starts with a different device, so this published example is not proof of latest-record ordering. Use the example to review product-description and source-reference observations. The tool does not certify device safety, determine applicability to an individual device, provide clinical advice or establish complete global recall coverage. Consult authoritative FDA notices for decisions. The Actor lists USD0.02 per billed row; check current Apify billing and input instructions before running. No fresh paid Actor run was performed for this submission. Published by ZentraFoundry, part of Nimblique Studio, with AI-assisted copy. Direct buyer URL: https://apify.com/zentrafoundry/fda-safety-signal-monitor

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Who should use openFDA Device Enforcement Snapshot — ZentraFoundry?

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Pricing: Paid

Platforms: Web

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Paid Check the provider’s own page for the latest pricing, packages and terms.

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Details, pricing and availability can change. We use provider information, verified owner updates and editorial review where available. Check the provider’s own page before making a purchase, booking or important decision.

Profile last updated 14 Oct 2026.
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