Software

In this episode, host Shikha Jain, MD, speaks with Annmarie Ison about developing safe and accurate software, how software can improve health care disparities and more.

LAS VEGAS — CSI Dry Eye Software has launched new technology that uses AI to assist clinicians in making a dry eye diagnosis and developing a treatment plan, according to a company executive at Vision Expo West.

Digital health company Luminopia Inc. announced real-world data from the Patients Using Prescription Luminopia Registry, which demonstrated the efficacy of its binocular, virtual reality-based medical device for children with amblyopia.

Large volume infusion pump software related to the Ivenix Infusion System has been recalled by its manufacturer due to multiple potentially dangerous issues, according to a press release from the FDA.

The FDA has granted 510(k) clearance to LungQ 3.0.0, an artificial intelligence-based software that identifies different parts of lung anatomy and evaluates lung tissue and fissure completeness, according to a press release.

The FDA has granted 510(k) clearance to CT LVAS, a software that provides information on patient lung function that can be interpreted alongside lung structural details obtained during CT scans, according to a press release.

A Bay Area neurotechnology firm has announced the commercial release of a novel artificial intelligence-based software algorithm that continuously monitors brain activity of those with electrographic status epilepticus.

Bausch + Lomb introduced new surgical planning software for the Eyetelligence platform.

Use of artificial intelligence triage software led to a significant reduction in 30- and 120-day all-cause mortality for those with intracranial hemorrhage compared with those treated without the algorithm, according to research.

Altris AI’s IMS platform, which can store and organize OCT scans and supports improved analysis, has received FDA 510(k) clearance, the company announced in a press release.