FDA 510(k) Competitor Clearance Tracker

openFDA 510(k) Device Clearances Scraper

automation-lab/openfda-510k-device-clearances-scraper

Export FDA 510(k) medical device clearance records by applicant, product code, k-number, decision date, and clearance metadata.

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

ryanclinton/fda-510k-clearances

Search the FDA's database of **174,000+ 510(k) premarket notification clearances** for medical devices. Filter by device name, company, product code, advisory committee, decision type, clearance type, date range, or country.

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.

FDA 510(k) Scraper: Device Clearances

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.

FDA Data Scraper - openFDA Recalls & Events

logiover/fda-data-scraper

openFDA data export tool: scrape FDA drug recalls, adverse events, drug labels and 510(k) clearances to CSV or JSON. No API key, no login required.

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

Medtech peer benchmarking intelligence for AI agents. Compare device manufacturers safety profiles against product-code peers using FDA MAUDE, 510(k), and enforcement data.

OpenFDA Adverse Events & Recalls Extractor

xtracto/openfda-events

Extract FDA drug/device adverse events (FAERS/MAUDE), recalls, and 510(k) clearances — one record per row. Tens of millions of records available. Public FDA data, no login.