FDA Medical Device Manufacturer Leads: Registered Firms

FDA Medical Device Recalls Scraper

automation-lab/fda-medical-device-recalls-scraper

Extract official FDA medical device recall records from openFDA by firm, product, class, status, location, and date. Export JSON, CSV, or Excel.

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.

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.

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 Medical Device Establishment Registration Scraper

automation-lab/fda-device-registration-scraper

Export FDA device establishment registrations, FEI numbers, owner/operators, addresses, product codes, classes, and 510(k)/PMA refs from openFDA.

FDA Recalls Scraper - Drug, Device & Food

maydit/us-fda-recalls-scraper

Scrape & monitor FDA drug, medical device, and food recalls from the openFDA enforcement API in one run. Filter by type, class, state, and date. Export CSV/JSON.

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.

FDA MAUDE Adverse Event Reports Scraper

automation-lab/fda-maude-adverse-event-reports-scraper

Extract FDA MAUDE medical device adverse event reports by date, manufacturer, device, product code, event type, or MDR identifiers.

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

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.