SyncThink gets FDA approval for eye-tracking device to test for concussions in 60 seconds
SyncThink, a company that has led the field of eye tracking technology, has announced that it has received FDA clearance for its medical device, EYE-SYNC, which uses infrared cameras to determine within 60 seconds if someone has endured a concussion.
Concern about concussions is clearly a very public issue now for athletes. By measuring visual target motion, this handheld, virtual reality, eye-tracking technology can determine whether an athlete has been concussed. It’s often faster than a medical examiner, the company said.
SyncThink, which has headquarters and research staff in Boston, New York and Palo Alto, collaborated with the Brain Trauma Foundation in developing this device.
“In my opinion, the EYE-SYNC device has significant implications for sideline evaluation, and I can see in the future how this can be the diagnostic gold standard for sports related concussion with every pro, college and high school team having one on the field,” Scott Anderson, director of athletic training for Stanford University Sports Medicine, said in a SyncThink statement.
Anderson said that Stanford Sports Medicine is testing EYE-SYNC as an investigational device to screen athletes for concussions and help decide if it is safe for them to return to play.
SyncThink claims more than 40 peer-reviewed research articles demonstrating the effectiveness of the device, plus 10 patents and a database of more than 10,000 people who have been tested with EYE-SYNC.
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