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FDA Clears Sentec’s LuMon System for Bedside Lung Imaging

The LuMon system provides real-time, radiation-free lung imaging for premature infants, children, and adults, helping clinicians tailor respiratory therapy at the bedside.

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GE HealthCare Leads FDA AI Device Clearances for Fourth Consecutive Year

The company has now accumulated over 100 authorizations for artificial intelligence in its medical technology portfolio.

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FDA Clears AI Tool for Detecting Low Ejection Fraction from ECGs

The software analyzes 12-lead ECGs to detect signs of low left ventricular ejection fraction in patients at risk of heart failure.

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FDA Clears Sentec’s LuMon System for Bedside Lung Imaging

The LuMon system provides real-time, radiation-free lung imaging for premature infants, children, and adults, helping clinicians tailor respiratory therapy at the bedside.

New MRI-Compatible Infusion Pump Receives FDA Clearance

May 29, 2025

Designed for use in MRI environments, the infusion pump builds on the company’s earlier systems, which the company says remain the only non-magnetic infusion pumps cleared for use during MRI procedures.