Device Events – Improve Patient Outcomes & Reduce Risk Through Better Information.

Improve Patient Outcomes & Reduce Risk
Through Better Information.
Mission Statement
Our mission is to contribute to better patient outcomes and improve patient safety while reducing the risk associated with medical device decisions by healthcare organization and providers.

We empower users with information to make more informed decisions about the medical devices they use, before device recalls are issued by the FDA.
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.
Our Value
We enable healthcare organizations to:
• Improve overall quality, patient outcomes and safety
• Reduced risk associated with problematic devices
Who We Help
Healthcare Organizations including personnel in:
• Procurement
• Clinical Quality
• Risk Management
• Legal
• Patient Outcomes
• Compliance