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$2.00 / 1,000 results

FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE

Unified FDA device data: 510(k) clearances, PMA approvals, recalls, MAUDE adverse events & classification. Normalized manufacturer names, cleaned device names, specialty mapping. 175K+ records, free openFDA API.

Pricing

$2.00 / 1,000 results

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Chris Wakefield

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5 days ago

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FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE API through CLI

The Apify CLI is the official tool that allows you to use FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE locally, providing convenience functions and automatic retries on errors.

Install Apify CLI

Using installation script (macOS/Linux):

$curl -fsSL https://apify.com/install-cli.sh | bash

Using installation script (Windows):

$irm https://apify.com/install-cli.ps1 | iex

Using Homebrew:

$brew install apify-cli

Using npm:

$npm install -g apify-cli

Other API clients include:

FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE API in Python

FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE API in JavaScript

FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE OpenAPI definition

FDA Medical Device Database — 510(k), PMA, Recalls & MAUDE API

openFDA Medical Device Adverse Events & Recalls Scraper

scrapers_lat/openfda-device-events-scraper

Scrape FDA medical device adverse events (MAUDE), device recalls and 510(k) clearances from the official openFDA API. Extract report number, device brand, manufacturer, event type, product problems and dates across the United States. Export to JSON, CSV or Excel.

Scrapers Lat

5.0

💊 FDA Intelligence — Recalls, Approvals & Adverse Events

inexhaustible_glass/fda-intelligence-scraper

Scrape ALL FDA open data (openFDA): drug & device recalls, adverse events (FAERS/MAUDE), labels, device clearances (510k) & approvals (PMA), food recalls. 40M+ records, filter by date & field. For pharma, devices, product-liability lawyers, insurers, investors. Free, no key, no proxy.

Hitman studio

Healthcare Compliance MCP — AI Agent FDA Device Intelligence

red.cars/healthcare-compliance-mcp

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

AutomateLab

Medical Device Records — FDA 510(k) & PMA API

nexgendata/medical-device-fda-intelligence

Track FDA medical device 510(k) clearances and recalls from official openFDA data: applicant, device, product code, class, decision date, and Class I/II/III recall severity. For medtech intelligence.

NexGenData

FDA 510k Device Clearance Monitor

technicaldost/fda-device-510k-monitor

Track recent medical device 510(k) clearances from openFDA.

Technical Dost Solutions

FDA MAUDE Device Event Monitor

technicaldost/fda-maude-device-events-monitor

Monitor medical device adverse events from openFDA MAUDE data.

Technical Dost Solutions

OpenFDA Adverse Events & Recalls Extractor

xtracto/openfda-events

Extract FDA drug/device adverse events (FAERS/MAUDE), recalls, and 510(k) clearances — one record per row. Tens of millions of records available. Public FDA data, no login.

Farhan Febrian Nauval

FDA PMA Medical Device Approvals Scraper

automation-lab/fda-pma-medical-device-approvals-scraper

Export FDA PMA approvals and supplement records from openFDA for regulatory monitoring, medtech intelligence, and device research.

Stas Persiianenko

US FDA Compliance Monitor

great_pistachio/us-fda-compliance-monitor

Monitor the FDA for medical device recalls, 510(k) clearances, PMA approvals, and drug/food enforcement actions, from the official openFDA API. Filter by firm, product, or keyword and date. For regulatory affairs, compliance teams, and competitive intelligence.