The U.S. Food and Drug Administration has cleared a new medical device invented by a Twin Cities neurosurgeon to detect signs of concussion by tracking a patient’s eye movements.
The device, called the EyeBox, was invented by Minnesota neurosurgeon Dr. Uzma Samadani following the discovery that slight discrepancies in how a patient’s eyes track an image on a screen can reveal a wealth of information about underlying brain dysfunction.
Oculogica, the device’s New York-based maker, commercially launched the EyeBox on Thursday after years of clinical testing led to FDA clearance on Dec. 28. The price of the device is not being disclosed. It’s intended only for physician use for now.
The EyeBox works by tracking a person’s eyes as he or she watches a 4-minute video clip that “bounces” around a large screen. Different types of discrepancies in eye movements while watching something in motion can reveal potential brain problems, including concussions, researchers have found.
Unlike traditional concussion tests, the results of an EyeBox exam are quantifiable and don’t depend on comparison to a “baseline” concussion test, which can be manipulated by athletes or soldiers who want to avoid being diagnosed with brain injury.
In the long run, the device’s major contribution may be to create an objective measurement for classification of different types of brain injuries, Samadani said in an interview. For now, though, the device has one use—aiding a doctor’s judgment in deciding whether a patient has a concussion. The FDA clearance said doctors can use the device on patients ages 5 to 67 within a week of sustaining a concussion.
“Oculogica is the first to use eye-tracking technology and their sophisticated algorithms to transform how concussions and mild traumatic brain injuries are diagnosed, particularly since no baseline is required,” wrote Lisa Crump, a partner with Minneapolis investment firm Sofia Fund, which has invested in Oculogica through three funding rounds. “They are the first to demonstrate and get approval to utilize the technology in assisting with the medical diagnoses of concussions.”
The EyeBox was cleared for marketing through the FDA’s “de novo” classification program, intended for lower-risk medical devices that have no direct predecessors in regulatory files.
Someday, Samadani said, the device could probably become a widely used consumer device. Oculogica’s announcement of the FDA clearance noted that large consumer-tech companies including Google, Apple, Samsung and Facebook have made investments in eye-tracking technologies since 2016, and all have expressed an interest in the health care industry.
“Certainly a consumer device that could help people make decisions at home would be great. But that is not where we are yet,” Samadani said.
Samadani, a University of Minnesota associate professor in neurosurgery, is a founder and a board member of Oculogica, but she has not worked as an employee of the company since 2015. Her sister Rosina Samadani, a biomedical engineer with a business background, is the CEO.
Rosina Samadani noted that a small number of the devices are in the field already, at clinical trial sites including the Mayo Clinic in Minnesota.
“For this first year we are trying to place devices with knowledgeable pilot sites,” Rosina Samadani said in an interview. “We’ve done well with our clinical study sites, and we sort of want to continue in that vein early on here, and make sure that we are working with specialists who really understand concussion. And then we will have a much bigger sales effort once we’ve got this initial foothold.”
Although the EyeBox has a revenue stream—hospitals can bill for use of the device under existing medical codes, and Oculogica is working on a unique code for the EyeBox—don’t expect to see the device on the sidelines of a high school football game soon.
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