FDA Medical Device Alert Monitor

EUDAMED Medical Device Companies Scraper

scrapers_lat/eudamed-medical-device-actors-scraper

Directory of EU EUDAMED-registered medical device operators: manufacturers, authorised reps, importers and pack producers with email, phone, EU VAT, EORI, trade register number and named regulatory-compliance contacts. JSON, CSV, Excel.

FDA Drug Shortages Monitor — Current & Resolved API

nexgendata/fda-drug-shortages-monitor

Monitor current & resolved FDA (CDER) drug shortages with drug, manufacturer, status, availability, category and dates. For hospital pharmacy, GPOs, 503B compounders, and pharma supply chain.

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.

FDA 510(k) Scraper - Medical Device Clearance API

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

Search FDA 510(k) medical device clearances via the official OpenFDA API. Use this scraper/API to find cleared devices by name, applicant, product code, or decision date and monitor competitor approvals, regulatory decisions, and predicate devices. No FDA API key needed.

MHRA UK Drug & Device Safety Alerts & Recalls Scraper

scrapers_lat/mhra-drug-device-alerts-scraper

Scrape MHRA UK drug & medical device safety alerts and recalls: Field Safety Notices, National Patient Safety Alerts, Device Safety Information, medicines recalls. Filter by alert type, date, keyword, product.

FDA Catalyst Alerts

constant_quadruped/fda-catalyst-alerts

Monitor FDA catalysts for biotech trading signals. Track PDUFA dates, Phase 3 completions, AdCom meetings, safety signals, and recalls. Get alerts via webhook when catalysts approach. Includes 100+ pharma ticker mappings. Schedule daily for continuous portfolio monitoring.

Live openFDA drug enforcement rows (Try: Clindamycin Injection). US FDA only. Not a safety certification. $0.02 / row.

Extract and normalize FDA medical device recall data with risk classification and company intelligence.

Scrapes FDA's official Section 506J medical device shortage list and device discontinuance list into structured records.

Scrapes FDA's official list of AI/ML-enabled medical devices authorized for U.S. marketing into structured records.