FDA 510(k) Device Clearances

FDA 510k Device Clearance Monitor

technicaldost/fda-device-510k-monitor

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

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.

Per-record FDA 510(k) medical-device clearances from the official openFDA API. Applicant, device, product code, decision, dates, class. Keyless, public domain, no personal data.

FDA 510(k) Premarket Clearances Scraper

scrapers_lat/fda-510k-clearances-scraper

Scrape FDA 510(k) premarket clearances from the official openFDA database. Filter by device, applicant, product code, medical specialty, state, country, clearance type and decision date. Enrich with device class and regulation. Export JSON, CSV, Excel.

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.

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.

Query FDA MAUDE adverse events, 510(k) clearances, and device recalls. One tool call for AI agent medical device compliance research.

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.

Export openFDA 510(k) premarket device clearance records — applicant, device name, decision date and code, product code, advisory committee, device class and regulation number — filterable by applicant, device, product code, committee, class or decision-date range, as clean JSON, CSV or Excel.

Unified FDA device data: 510(k) clearances, PMA approvals, recalls, MAUDE adverse events & classification. Normalized manufacturer names, cleaned device names, specialty mapping. 175K+ records, free openFDA API.