FDA 510(k) Medical Device Clearance Radar (Save 90%)

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 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.

FDA 510k Device Clearance Monitor

technicaldost/fda-device-510k-monitor

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

Lead lists of FDA-registered medical device establishments: filter by state, product code, and establishment type, and get one row per firm with address, the official correspondent's name and phone, and the devices it makes. Keyless official FDA API, no browser. Pay per manufacturer.

FDA 510(k) Clearances Scraper | 11 Fields, No API Key

themineworks/fda-510k-device-clearances

Scrape FDA 510(k) medical device clearances by company, device, or product code. Returns applicant, decision date, decision type & panel for medtech competitive intel and regulatory affairs. No API key. Use it as an MCP server in Claude, ChatGPT & AI agents.

Search FDA medical device registrations — 510(k) clearances, PMA approvals, device classifications. Medtech intelligence, regulatory compliance, competitive analysis.

FDA MAUDE Medical Device Adverse Events Scraper API

pink_comic/fda-maude-device-events

Search FDA MAUDE adverse-event reports by report, manufacturer, device, product code, event, dates, patient outcome, and device problem. Returns source-linked nested device and patient evidence with mandatory non-causation limits.

FDA 510(k) Device Clearances Scraper

nexgenwatch/fda-510k-device-clearances

Clean, structured records of medical-device 510(k) clearances, sourced live from the official openFDA device 510(k) API (https://api.fda.gov/device/510k.json) — an anonymous, documented U.S. Food & Drug Administration endpoint.

US FDA Compliance Monitor

great_pistachio/us-fda-compliance-monitor

Monitor the FDA for medical device recalls, 510(k) clearances, PMA approvals, and drug/food enforcement actions, from the official openFDA API. Filter by firm, product, or keyword and date. For regulatory affairs, compliance teams, and competitive intelligence.