FDA Medical Device Suppliers & Manufacturers Finder

This FDA medical device supplier finder turns the FDA's establishment registration and device listing database into clean supplier lists: type a device such as catheter, surgical mask or orthopedic implant, pick countries, and get one row per device listing with the registered firm, its address, owner company, role (manufacturer, contract manufacturer, sterilizer, repackager, exporter), brand names, FDA product codes, device class and 510(k) or PMA number.

Use it as a medical device manufacturer directory, an FDA registration lookup API, a contract manufacturer finder for white-label sourcing, or a competitor map of who sells a device type into the US, from your own code, Make, Zapier, n8n or an AI agent.

It reads the official openFDA API (api.fda.gov/device/registrationlisting), with no browser and no login. The prefilled demo returns 20 rows. $0.75 per 1,000 results, no start fee.

What goes in: device words, and optional filters on country, US state, establishment role, FDA product code, device class, medical specialty or company name. What comes out: one row per device listing (or one per supplier, with a switch). When to use it: you need to know which firms are registered with the FDA to make or handle a device type, where they are, and what else they list.

What it does not have: no prices, no minimum order quantities, no e-mails and no phone numbers. The FDA file names people (US agents, official correspondents) with their phone and e-mail; this actor leaves all of that out on purpose and keeps only company data.

What you get

• Supplier: registered establishment name, FDA registration number, FEI number, street, city, state, postal code, country.
• Owner: owner/operator company and number (groups all sites of one parent), owner city and country; the US agent's company name for foreign sites.
• Role: what the site does, e.g. "Manufacture Medical Device", "Manufacture Medical Device for Another Party (Contract Manufacturer)", "Sterilize Medical Device for Another Party (Contract Sterilizer)", "Repack or Relabel Medical Device".
• Devices: brand / proprietary names, FDA product codes, generic device names, device class, review panel (medical specialty), 21 CFR regulation number, listing date per product.
• Regulatory: 510(k) number or PMA number on the listing, registration year, initial-importer flag.

Fill rates in a 2,500-row test (catheter, all countries, run 5 November 2026): firm, registration, address, city, owner, role, product codes, device names and class 100%; brand names 78%; 510(k) number 50%; US agent company 32% (foreign sites); PMA number 1%. Country mix: US 1,457, MX 203, CN 143, CA 76, CR 75, IE 60, GB 49, DE 41. 817 different registered sites.

Sample output

Real rows from the prefilled run (catheter, Germany, manufacturers, 5 November 2026), a few of the 27 fields, long device names shortened:

firm	city	brand names	device	code	class	510(k)
AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg	Aesculap	Catheter, Irrigation	GBX	1
Contract Medical International GmbH	DRESDEN Saxony	Fortress	Introducer, Catheter / Dilator, Vessel	DYB, DRE	2	K203179
BIOTRONIK SE & CO. KG	BERLIN	Selectra 3D-65-39 (and 7 more)	Catheter, Percutaneous	DQY	2	K193474
B. BRAUN MELSUNGEN AG	MELSUNGEN Hesse	Perifix ONE Pediatric Catheter	Catheter, Conduction, Anesthetic	BSO	2	K090884
VYGON Germany GmbH	AACHEN North Rhine-Westphalia	Multicath Expert	Catheter, Intravascular, Therapeutic, Short-Term	FOZ	2	K061250

Use cases

• Supplier sourcing: find registered manufacturers or contract manufacturers of a device type, by country
• White-label / OEM search: filter on the contract manufacturer role to find sites that make devices for other brands
• Competitor mapping: who lists a product code, under which brands, and where they make it
• Due diligence: check that a supplier is registered, what it lists and whether a 510(k) is on file
• Lead generation for suppliers to the industry: lists of device makers by specialty and country (company data only)

Pricing

$0.75 per 1,000 results (pay per result, $0.00075 each), no start fee, platform usage included. A result is one row saved to your dataset. Searches that find nothing, duplicates, rows skipped by "one row per supplier" and failed requests are never charged. Set Max results per search to cap the cost of a run.

The data comes from a free public API. You pay for the ready rows, the filters and the clean company-only output, not for access. If you prefer, call openFDA yourself.

Nearest Store actors on 21 October 2026 (Apify Store snapshot): a general openFDA scraper for recalls, labels and adverse events at $1.60 per 1,000 (free tier) down to $0.80 (gold), with no registration / supplier search. Prices change; check before you compare.

FAQ

Where does the data come from? The FDA's establishment registration and device listing file, served by openFDA. openFDA data is public domain (CC0); the FDA asks for, but does not require, the credit "Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)". The FDA says not to rely on openFDA for medical decisions and that results are unvalidated.

How fresh is it? As fresh as openFDA. On 5 November 2026 the API reported last_updated 2026-10-26.

Does it include phone numbers or e-mails? No. The FDA file holds the names, phones and e-mails of people (US agents, official correspondents). The actor never copies them. You get company names and site addresses.

Is a listing a product I can buy? A listing says a firm is registered to make or handle a device type for the US market. It is not a catalogue entry, and it has no price or stock.

Does a 510(k) number mean the device is cleared? It is the number filed on the listing. Check the FDA's 510(k) database before relying on it.

How do I get one row per company? Turn on One row per supplier. The first listing of each registered site is kept; the rest are read but not charged.

What does "U", "N" or "f" mean in device class? Values the FDA file holds besides 1, 2 and 3. The actor passes them through as filed.

Are there limits? openFDA allows 240 requests a minute and, without a key, 1,000 requests a day per IP. Each request returns up to 1,000 rows, so normal runs use a handful. If you run very large jobs, add your free openFDA key in openFDA API key; it is sent in a header and never written to the log.

Why are some cities odd, like "TUTTLINGEN, DONAU Baden-Wurttemberg"? That is how the firm filed it. The actor does not rewrite addresses.

Known gaps: one row per listing means a big firm appears many times (use the supplier switch); the address is the registered site, which can be a plant rather than a sales office; firms that are not registered with the FDA are not in it; device words match the FDA generic name and the brand name only, not marketing text. Runs above about 25,000 rows per search were not tested.

How to use

1. Open the actor and type one or more device words, e.g. catheter.
2. Optional: set countries (DE, CN), a role (Manufacture Medical Device), product codes or device class.
3. Set Max results per search (start with 20).
4. Click Start, then export the dataset as CSV, Excel or JSON.

Input

Field	What it does
searchTerms	Device words; each runs as its own search on the FDA device name and the brand name.
countries, states	ISO country codes, US state codes. Any of them matches.
establishmentTypes	FDA roles, e.g. manufacturer, contract manufacturer, sterilizer, repackager.
productCodes, deviceClasses, medicalSpecialties	FDA product codes, class 1 / 2 / 3, review panel.
firmNames	Find what one company lists (establishment or owner name).
uniqueSuppliers	One row per registered site instead of per listing.
maxResultsPerSearch	Rows per search; 0 = all.
apiKey	Optional free openFDA key (secret).

Invalid filter values are ignored and listed in the run summary. A filter where no value is valid stops the run instead of widening the search.

Input example

{
    "searchTerms": ["catheter", "surgical mask"],
    "countries": ["DE", "CN"],
    "establishmentTypes": ["Manufacture Medical Device"],
    "deviceClasses": ["2"],
    "maxResultsPerSearch": 200
}

Output example

One real row from the prefilled run (5 November 2026):

{
    "firmName": "AESCULAP AG",
    "registrationNumber": "9610612",
    "feiNumber": "3002806315",
    "establishmentTypes": ["Manufacture Medical Device"],
    "street": "AM AESCULAP PLATZ",
    "city": "TUTTLINGEN, DONAU Baden-Wurttemberg",
    "state": null,
    "postalCode": "D-78532",
    "countryCode": "DE",
    "ownerOperatorName": "Aesculap AG",
    "ownerOperatorNumber": "8010193",
    "ownerCity": "Tuttlingen",
    "ownerCountryCode": "DE",
    "usAgentCompany": "Aesculap, Inc.",
    "initialImporter": false,
    "registrationExpiryYear": 2027,
    "deviceBrandNames": ["Aesculap"],
    "productCodes": ["GBX"],
    "deviceNames": ["Catheter, Irrigation"],
    "deviceClasses": ["1"],
    "medicalSpecialties": ["General, Plastic Surgery"],
    "premarketNumber510k": null,
    "premarketApprovalNumber": null,
    "products": [
        {
            "productCode": "GBX",
            "deviceName": "Catheter, Irrigation",
            "deviceClass": "1",
            "medicalSpecialty": "General, Plastic Surgery",
            "regulationNumber": "878.4200",
            "listedDate": "2008-07-30",
            "exempt": null
        }
    ],
    "searchTerm": "catheter",
    "position": 1,
    "scrapedAt": "2026-11-05T18:31:44.876Z"
}

A RUN_SUMMARY record in the key-value store lists, per search, how many listings match, how many were saved, why the search stopped and any input that was ignored.

Integrations

Export the dataset as JSON, CSV, Excel, XML or HTML, or pull it with the Apify API and the JavaScript / Python clients. Connect it to Make, Zapier, n8n, Google Sheets, HubSpot or Slack with Apify integrations and webhooks, or let an AI agent call it through the Apify MCP server.

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