By utilizing three wavelength channels, as well as OCT scanning, the Optos Silverstone RGB retinal imaging device allows for ...

Toku’s AI (CLAiR) technology platform has received FDA Breakthrough Device status, and if cleared by the FDA will deliver real-time cardiovascular disease (CVD) risk assessments through routine eye ...

A new study has proposed that a simple retina scan could indicate whether a person is at risk of early death. The research found the greater the gap between a person’s chronological age and retinal ...

The Associated Press LONDON -- A new high school said Wednesday its students will be charged for their lunches with a retina scanning device to prevent poor children who eat for free from being ...

Inherited retinal diseases (IRDs), single-gene disorders affecting the retina, are very difficult to diagnose since they are uncommon and involve changes in one of many candidate genes. Outside ...

Using an algorithm developed by Duke researchers, scientists were able to correctly identify retinal scans of people with mild cognitive impairment about 79% of the time. File photo Researchers have ...

Researchers have identified novel retinal vascular signatures that are significantly associated with the risk for a first stroke. When combined with age and sex, these retinal “fingerprints” predicted ...

Toku Eyes, a New Zealand-based healthcare AI company, is launching its tool that assesses heart risk through a retinal scan in the U.S. The tool, called ORAiCLE, uses an AI platform to identify ...

The retina is the only organ where blood vessels are directly seen without any invasive measures. A South Korean startup, Mediwhale, wants to use artificial intelligence (AI) to diagnose kidney ...

A Rose Hill-based company is taking a shot at decentralizing the shrinking field of ophthalmology. AI Optics, a biotech startup backed by NYU Langone and raising in stealth, announced clearance this ...

Glasgow, UK: Inherited retinal diseases (IRDs), single-gene disorders affecting the retina, are very difficult to diagnose since they are uncommon and involve changes in one of many candidate genes.