FDA MAUDE Intelligence MCP

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

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.

FDA 510(k) Device Clearance Monitor

pink_comic/fda-510k-medical-device-clearances

Monitor new FDA 510(k) medical device clearances daily. Schedule runs to track clearances by device type, applicant, or product code. For medtech companies, investors, regulatory consultants, and competitive intelligence. Pay per result.

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

FDA 510(k) Device Clearance Search

ryanclinton/fda-510k-clearances

Search the FDA's database of **174,000+ 510(k) premarket notification clearances** for medical devices. Filter by device name, company, product code, advisory committee, decision type, clearance type, date range, or country.

Extracts FDA recall and enforcement data for drugs, food, and medical devices using the openFDA API. Filter by product type, classification, date range.

FDA Recalls Scraper

automation-lab/fda-recalls-scraper

Search FDA enforcement database for drug, food, and medical device recalls. Get recall classifications, reasons, product descriptions, and distribution data.

Monitor FDA recalls, safety alerts, and enforcement actions for drugs, medical devices, and food products. Stay compliant with automated recall tracking and notifications.

FDA Device Recalls — MedTech CI & PV Lookup API

azureblue/medical-device-recall-scraper

Fetch FDA medical device recall records via OpenFDA. Filter by device name and date. Returns recall number, reason, risk class, company and recall status.

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.