US Medical Device Clearances — 510(k) & PMA Decisions

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.

Scrape EU-registered medical devices from EUDAMED (2.6M+). Device, risk class, status, manufacturer & EU authorised representative. MDR/IVDR compliance & medtech leads. Free, no key, no proxy.

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.

Medical Device Records — FDA 510(k) & PMA API

nexgendata/medical-device-fda-intelligence

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.

FDA 510(k) Device Clearance Search

maximedupre/fda-510k

Search official FDA 510(k) clearances and save structured device, applicant, decision, classification, review, and source data. You can also rank matching clearances by applicant, year, device class, or product code.

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

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.

FDA 510(k) Device Clearance Research

ledgerstar/fda-device-clearances

Corporate supplier research from FDA 510(k) substantial-equivalence decision records. A clearance is not described as FDA approval.

Sub-second regulatory intelligence tracking new Premarket Notifications (510k) cleared by FDA. Monitors medical device competitors, product clearances, and applicant sponsors.

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