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FDA Device Establishment Registration — Bulk Supplier Lookup

Look up FDA device establishment registration records in bulk. Screen a supplier list by firm name, registration number, FEI number or owner/operator number and get registration status, establishment types, US agent and every listed device with product code, device class and CFR regulation.

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from $0.01 / 1,000 results

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Malek H

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FDA Device Establishment Registration — Bulk Lookup API through CLI

The Apify CLI is the official tool that allows you to use FDA Device Establishment Registration — Bulk Supplier Lookup locally, providing convenience functions and automatic retries on errors.

Install Apify CLI

Using installation script (macOS/Linux):

$curl -fsSL https://apify.com/install-cli.sh | bash

Using installation script (Windows):

$irm https://apify.com/install-cli.ps1 | iex

Using Homebrew:

$brew install apify-cli

Using npm:

$npm install -g apify-cli

Other API clients include:

FDA Device Establishment Registration — Bulk Supplier Lookup API in Python

FDA Device Establishment Registration — Bulk Supplier Lookup API in JavaScript

FDA Device Establishment Registration — Bulk Supplier Lookup OpenAPI definition

FDA Device Establishment Registration — Bulk Supplier Lookup API

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.

Stas Persiianenko

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.

azureblue

FDA Medical Device Manufacturer Leads: Registered Firms

scrapemint/fda-device-manufacturer-leads

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.

Ken M

Fda Establishment Inspections Scraper

chimerical_quicklime/fda-establishment-inspections-scraper

Pull FDA-published establishment recall and enforcement records (drug, food, or device). Wraps the official openFDA REST API. Outputs recalling firm, product description, recall classification, distribution pattern, and dates — ready for compliance, due diligence, and pharma/manufacturing intel.

Khrystyna Skotte

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

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.

Ryan Clinton

FDA Recalls Scraper — Drug, Device & Food

ponderable_hydrometer/fda-recalls-scraper

Track FDA drug, device and food recalls via the official openFDA API. Filter by date, class or firm. Structured data: firm, reason, class, status. Free, no key.

Ponderable Hydrometer

FDA Device Recall Intelligence

skootle/fda-device-recall-intelligence

Official openFDA medical device recalls with product codes, device classes, K numbers, firms, root causes, actions, API output, schedules, monitoring, and integrations.

Skootle

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.

Ava Torres

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.