AccessGUDID Medical Device Records Scraper

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.

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.

Philadelphia L&I Business Licenses

nexgenwatch/philadelphia-li-business-licenses

One record per Philadelphia L&I business licence (licence number, type, status, business + legal name, issue/expiration/inactive dates, address, and the OPA property-owner context) from the City's Carto SQL endpoint.

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.

EIA-923 Generator-Unit Net Generation (Monthly, Preliminary)

nexgenwatch/eia923-generator-unit-net-generation

Structured generator-unit monthly net generation records from the U.S. EIA Form EIA-923 Page 4 Generator Data sheet, read directly from the official current-year monthly ZIP on www.eia.gov.

ECB HICP Inflation Series

nexgenwatch/ecb-hicp-inflation-series

Structured HICP (Harmonised Index of Consumer Prices) inflation series from the European Central Bank's official keyless SDMX Data Portal (data-api.ecb.europa.eu, the HICP dataflow).

UK Legislation Section Retrieval — legislation.gov.uk

nexgenwatch/uk-legislation-section-retrieval

Retrieve individual sections of UK legislation from the official legislation.gov.uk service.

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.

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