Quick Tour · 46 seconds
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A fast introduction for prospective customers evaluating the platform.
Medical Device Intelligence Platform
Device Intelligence for Regulatory & Quality Teams
Search adverse events, recalls, and 510(k) clearances through fast, AI-assisted dashboards built for medical device manufacturers.
18M+
FDA adverse event records
510(k)
clearance search
AI
summaries & insights
See Intelli-Data in Action
Explore the platform before you sign in
Start with the quick tour, then watch the platform overview for a closer look at how Intelli-Data turns FDA data into useful regulatory and quality intelligence.
Platform Overview · 1 minute 31 seconds
Discover what Intelli-Data can do
A fuller look at the platform's value for regulatory, quality, and risk teams.
Adverse Event Intelligence Platform
AI-powered adverse event intelligence
- AI-generated safety summaries
- Manufacturer normalization
- Competitive trend analysis
- Interactive adverse event dashboards
FDA Clearances
Compare clearances and intended use
Search by product code, applicant keyword, and decision date to identify device clearances and compare competitors. Review extracted intended use language alongside linked clearance documents to better understand positioning, regulatory history, and market activity.
Recall Intelligence
Monitor recalls in context
Query recall data by product description, classification, and date range to identify patterns and compare events across similar devices. Use recall intelligence to support competitive analysis, product monitoring, and broader quality and regulatory review.
FDA Device Intelligence
Built for Regulatory, Quality, and Competitive Intelligence Teams
Search millions of FDA adverse events, recalls, and 510(k) submissions through AI-assisted dashboards designed for medical device manufacturers.