Pricing

from $10.00 / 1,000 results

FDA MAUDE — Medical Device Adverse Event & Malfunction Reports

Search FDA MAUDE (Manufacturer and User Facility Device Experience) adverse event reports for medical devices. Report numbers, device names, manufacturer names, event types, dates, patient outcomes, and product problems. Official openFDA data, no API key.

Pricing

from $10.00 / 1,000 results

Rating

0.0

(0)

Developer

samwise.agency

Actor stats

Bookmarked

Total users

Monthly active users

20 hours ago

Last modified

What you get

Report number and event type
Device name and brand name
Manufacturer name
Event date and date reported to FDA
Patient outcomes (Death, Life-threatening, Hospitalization, etc.)
Product problems (Malfunction, Misuse, Labeling error, etc.)
Reporter occupation and location
Implant flag, device sequence number, UDI
Medical specialty and device class
Patient age and sex

Use cases

Medical device & imaging quality teams monitoring safety signals
Regulatory affairs professionals tracking adverse event trends
Product safety engineers identifying design flaws
Liability and insurance analysts assessing risk exposure
Health-IT integrators feeding safety data into clinical systems

Pay per report delivered.

Try it on Apify →

FDA Medical Device Adverse Event Search (MAUDE)

ryanclinton/fda-device-events

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.

Ryan Clinton

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

(1)

Fda Adverse Event Reporting Extract

jeeves_is_my_copilot/fda-adverse-event-reporting-extract

Public data actor with normalized output.

Alexander Abernathy

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.

ParseForge

Fda Adverse Events

jeeves_is_my_copilot/fda-adverse-events

Public data actor with normalized output.

Alexander Abernathy

FDA Adverse Events Scraper - FAERS + MAUDE Export

maydit/us-fda-adverse-events-scraper

Scrape FDA adverse events from FAERS (drugs) and MAUDE (devices) via openFDA. Deeply nested reports flattened to one clean row each. Export to CSV, JSON, or Excel.

Brandt May

FDA MAUDE Intelligence MCP

red.cars/fda-maude-intelligence-mcp

Medtech peer benchmarking intelligence for AI agents. Compare device manufacturers safety profiles against product-code peers using FDA MAUDE, 510(k), and enforcement data.

AutomateLab

Fda Intelligence Mcp

ryanclinton/fda-intelligence-mcp

Fda Intelligence Mcp. Available on the Apify Store with pay-per-event pricing.

Ryan Clinton

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

OpenFDA Intelligence MCP Server

andrew_avina/openfda-intelligence-mcp

The FDA's openFDA program contains over 20 million records across drug adverse events, recalls, product labels, medical device malfunction reports, and food enforcement actions. This data drives billion-dollar regulatory decisions â€” but the raw API is complex, inconsistently...