openFDA Medical Device Events Scraper

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

FDA MAUDE Device Event Monitor

technicaldost/fda-maude-device-events-monitor

Monitor medical device adverse events from openFDA MAUDE data.

FDA 510k Device Clearance Monitor

technicaldost/fda-device-510k-monitor

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

FDA Medical Device Recall Search

ryanclinton/fda-device-recalls

FDA Medical Device Recall Search queries the U.S. Food and Drug Administration's openFDA device enforcement endpoint to retrieve detailed, structured data about medical device recalls.

openFDA Medical Device Events Scraper

parseforge/openfda-device-event-scraper

Export MAUDE medical-device adverse-event reports from openFDA. Search 24M+ reports by device name, manufacturer, event type, and event-date range. Pull report ID, device, manufacturer, event narrative, patient outcome, and dates.

FDA Drug & Device Data Scraper (OpenFDA)

compute-edge/fda-openfda-scraper

Extract FDA drug approvals, adverse events, recalls, device clearances, and food recalls from the OpenFDA API. Search across 44M+ records with OpenFDA query syntax.

openFDA Drug & Device Data Crawler

jungle_synthesizer/openfda-drug-crawler

Crawl FDA drug adverse events, recalls, labels, NDC codes, device events, and 510(k) clearances from the openFDA API. Filter by drug name, manufacturer, date range, and severity. 20M+ adverse event reports available.

Extract FDA medical device classification entries from openFDA. Get product codes, device names, device class (I, II, III), regulation numbers, medical specialty, and regulatory flags. Filter by device class, medical specialty, product code, or regulation number.

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.

Search the FDA's **MAUDE database of 24 million+ medical device adverse event reports** — including malfunctions, injuries, and deaths. Filter by device name, manufacturer, product code, event type, report number, or date range.