Cognivue develops FDA-cleared digital cognitive assessment devices for earlier detection of potential cognitive impairment in healthcare settings. Conceived and developed in part by President and CEO Paul W. Estes beginning in 2009, its adaptive-psychophysics technology customizes self-administered testing to each patient’s visual and motor capabilities while collecting more than 130,000 data points. Based in Victor, New York, Cognivue supports clinical use and research through products including the five-minute Thrive screen and the more comprehensive Clarity assessment.
FDA-cleared technology
FDACLEARANCE
Quality certification