What We Do
Device Events is a cloud-based software alternative to the FDA MAUDE reporting service that provides easy to use, clear, comprehensive and cost-effective access to the most up to date information on adverse events involving medical devices.
We enable healthcare organizations, and the organizations that support them, to:
• Identify problem devices faster and earlier (before FDA recalls are issued).
• Understand the history, quantity and severity of associated adverse events.
• Access all the information on problems with specific devices.
• Make more informed decisions on selection and continued use of medical devices.
