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NovaSight Gains 510(k) Clearance for CureSight

October 5, 2022

NovaSight received 510(k) clearance from the FDA for its CureSight digital therapy device for treatment of amblyopia, also known as lazy eye.

The eye-tracking system trains users as they watch streamed video content of choice through red-blue treatment glasses. 

CureSight blurs the center of vision of the image that is shown to the strong eye using real-time image processing, which encourages the brain to complete the image's fine details from the lazy eye image and trains the two eyes to work as a team.

The FDA clearance was based on positive results from a clinical trial, which showed the digital therapy was noninferior to using a patch.

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