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About Us

Who We Are

Database Integration

Device Events LLC is a Pennsylvania-based company that provides a cloud-based software service that extracts, consolidates and provides clear and comprehensive metrics and reports on the millions of complex medical device adverse event reports (MDRs) and recalls that have been filed with the FDA.


Our service helps all organizations associated with healthcare by providing them with clear, comprehensive and cost effective access to the most up to date information on problem medical devices.


We are committed to making information on problem devices easily accessible to our customers so they can improve health outcomes and patient safety while reducing risk for their organizations.

Our History


Founded in 2015

Device Events LLC was founded by Madris Kinard in 2015. Through her previous work experience with the FDA and various consulting organizations, Madris identified that patient safety and health outcomes were being critically impacted by the inaccessibility of information on adverse events caused by medical devices.


Improving Outcomes

Through Device Events, Madris has made that information easily accessible through clear, comprehensive, metrics, reports and signal alerts that healthcare professionals can use to improve health outcomes and patient safety while reducing risk for their organizations.


Madris (Tomes) Kinard, MBA

Founder and CEO

Ms. Kinard is the pioneer and creative force behind Device Events, an innovative medical device surveillance and metric reporting system. Since the company’s founding in 2015, Ms. Kinard has been transforming the way patterns of adverse events in medical device usage are identified and tracked – a process that significantly helps healthcare professionals mitigate risk and make safer, more informed healthcare decisions for their patients.

Ms. Kinard’s expertise stems from an extensive background in public health. Prior to founding Device Events, she served as the FDA’s Adverse Events Subject Matter Expert for Devices and Unique Device Identification (UDI), where her leadership yielded two major initiatives. She spearheaded a team of architects in the development of a UDI system (the Global UDI Database), and oversaw the internal replacement of Manufacturer and User Facility Device Experience (MAUDE) (the Center for Devices and Radiological Health’s adverse event reporting system). She also expanded UDI stakeholder engagement, which attracted high-level representation from CMS, Kaiser Permanente, the National Committee of Vital Health Statistics (NCVHS), and the Joint Commission.

Ms. Kinard has made her mark as an industry expert and collaborates with several prominent teaching hospitals in adverse event reporting, device recall, and data quality troubleshooting. She co-authored
the American Heart Journal’s UDI Demonstration Abstract on Cardiac Stents with colleagues in public health from Mercy Health, the Mayo Clinic, Boston Scientific, Duke University, Medtronic, Abbott Laboratories, and the FDA. She currently heads a workgroup for the FDA’s Medical Device Epidemiology Network (MDEpiNet), which develops case studies on real-world device usage to improve the accurate identification of and communication about medical devices. Her latest coup for Device Events was clinching a $100,000 award for her efforts at the Rise of the Rest bus tour this fall, a campaign by AOL founder Steve Case’s venture fund “Revolution,” which supports entrepreneurs in emerging startup ecosystems across the country.

Her work has been featured on CNBC’s Power Lunch and CNN, and in the New York Times, Washington Post Magazine, and the British Medical Journal. She also maintains an active speaking schedule presenting to numerous FDA public workshops and industry conferences, educating healthcare audiences nationwide on topics ranging from UDI compliance to UDI in Meaningful Use and Claims.



Former FDA Unique Device Identification (UDI) External Program Manager

Former FDA Adverse Events Project Manager for Devices (MAUDE)

Medical Device Epidemiology Network (MDEpiNet) UDI Think Tank

MDEpiNet National Medical Device Registry Task Force & Catalog Number Workgroup

Medical Device Epidemiology Network 

Former CMS Consultant

Provider Enrollment Fraud and Abuse


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Contact Us

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