The market-leading medical device regulatory intelligence software. Every safety alert, regulatory change, and market signal aggregated from 27 regulators and delivered in under 90 seconds.
We parse 27 regulatory bodies, 140,000+ signals every month — classifying each as safety alert, regulatory change, market trend, clinical update, or supply event. No PDFs to skim. No RSS to babysit.
Pin every regulatory signal to the city it affects. See where an event landed, how many devices are exposed, and the nearest supply-chain risk.
Insights on medical device regulations, compliance, and market trends.
Search the FDA MAUDE database for medical device adverse event reports. How to query MAUDE, understand MDR reporting under 21 CFR 803, use the openFDA API, and set up real-time monitoring.
Read more →How to register medical devices in Japan with PMDA. 4-class system, Shonin vs 510(k), Ninsho certification, DMAL requirements, MHLW Ordinance 169 — complete comparison guide.
Read more →FDA launched AEMS in March 2026 to replace MAUDE, FAERS & 5 other databases. What changes for medical device teams — new features, timeline, API migration & what stays the same.
Read more →Free forever · No credit card · All 27 regulators