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BioWorld - Wednesday, March 4, 2026
Home » Topics » Medical devices » Digital health

Digital health
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Promise Bio founders

Promise Bio raises $8.3M for immune-mediated diseases platform

Dec. 17, 2024
By Shani Alexander
Promise Bio Ltd. emerged from stealth with $8.3 million in seed investment for its precision medicine platform, which addresses immune-mediated diseases.
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U.S. FDA headquarters

FDA’s AI PCCP final guidance relaxes indication for use restrictions

Dec. 9, 2024
By Mark McCarty
The FDA’s final guidance for predetermined change control plans (PCCPs) for AI products contains a number of editorial changes, some more significant than others.
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Mammogram

Mica AI looking to transform early breast cancer diagnosis

Dec. 3, 2024
By Shani Alexander
Mica AI Medical Ltd. is looking to transform the early diagnosis of breast cancer with its software which helps radiologists analyze mammograms more effectively. The company recently signed a collaboration and licensing agreement with Baptist Health South Florida in a bid to bring its technology to the U.S. market.
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Evie Ring - Movano

Movano rings up FDA pulse ox clearance for Eviemed

Dec. 2, 2024
By Annette Boyle
Movano Inc., dba Movano Health, added some clinical-grade glitz to its Evie ring with a U.S. FDA clearance for the built-in pulse oximeter. Movan’s stock shot up from an all-time low within minutes of the announcement on Dec. 2, as the clearance breathes new life into Movano’s plans to position the ring as a medical device.
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Ribbons of digital data

Hazards of prompt engineering a concern for regulation of GenAI

Nov. 26, 2024
By Mark McCarty
The health care potential for generative artificial intelligence comes with hazards such as the inadvertent effects of poor prompt engineering practices, but Anil Bhatta of Deloitte Consulting told a U.S. FDA advisory committee that this risk could be managed by rules that would thwart any consequent problems, such as an inadvertent jailbreak of the algorithm’s intended use.
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Female sitting on floor in dark room

Trivarx’s AI-based algorithm provides objective depression diagnosis

Nov. 26, 2024
By Tamra Sami
Diagnosing depression and other mental illnesses is largely subjective, but that could soon change as Sydney-based Trivarx Ltd. developed an AI-based algorithm that uses heart rate and heart rate variability coupled with sleep disturbance to diagnose major depressive episodes.
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Digital pills on a circuit board

FDA advisory panel sees heightened risk in connection with GenAI

Nov. 25, 2024
By Mark McCarty
The first day of the U.S. FDA’s two-day advisory hearing on generative artificial intelligence reflected some of the anxieties attached to this emerging technology, with the phenomenon of hallucinations driving several calls for more stringent regulation of this class of products that might be applied toward other entries in the class of artificial intelligence.
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Neurophet Aqua

Neurophet wins FDA nod for brain AI software, targets US expansion

Nov. 25, 2024
By Marian (YoonJee) Chu
On the heels of U.S. FDA approval for Neurophet Aqua, an updated version of its artificial intelligence (AI)-based magnetic resonance imaging analysis software for the brain, Neurophet Inc. is preparing for an IPO in 2025 and expansion into U.S. and European markets.
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Blood pressure gauge, ECG and medication

ISH position paper exhibits novel BP monitor tech

Nov. 21, 2024
By Marian (YoonJee) Chu
A new position paper from the International Society of Hypertension pinpoints the benefits and drawbacks of novel blood pressure management technology, including the latest cuff-based and cuffless and wearable devices like BP-measuring watches and rings.
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3D illustration of transparent human torso with close up of spinal cord

Nevro wins CE mark for spinal cord stimulation technology

Nov. 13, 2024
By Shani Alexander
Nevro Corp. received CE mark certification for its HFX iQ spinal cord stimulation system that delivers pain relief.
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