What You Should Know:
– Withings, a global leader in connected health, has announced that its Sleep Rx sleep apnea device has received clearance from the U.S. Food and Drug Administration (FDA).
– Sleep Rx represents…
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Introduction
Lung cancer remains one of the leading causes of cancer-related deaths worldwide, primarily due to the challenges in early detection and monitoring. However, the recent advancements in artificial intelligence (AI) are revolutionizing lung cancer…
What You Should Know:
– Qure.ai, a global innovator in medical imaging AI, has today announced a pivotal 510(k) FDA clearance for its AI-powered chest CT solution – qCT LN Quant.
– The new AI solution is now…
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What You Should Know:
– AISAP, a medical technology company specializing in AI-powered point-of-care assisted diagnosis (POCAD) solutions, announced today that it has received FDA 510(k) clearance for its groundbreaking CARDIO software platform.
– AISAP CARDIO…
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Some of the world’s most impactful companies were founded by college-aged visionaries — think Facebook, Microsoft and Dell. While it is unlikely that Brooklyn-based Cresilon will achieve levels of size and influence as grand…
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The proposed new Medicare billing codes in the proposed Physician Fee Schedule (PFS) for 2025 include three specific codes for digital mental health treatment (DMHT) relating to professional services involving DMHT devices. This is…
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What You Should Know: – TytoCare, a virtual care company enabling accessible, high-quality primary care from home, announced today that it has received an additional FDA clearance for a new AI-powered diagnostic capability, Tyto Insights…
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What You Should Know: – LG Electronics launches its latest addition to its diagnostic monitor lineup, the 21HQ613D-B. This 21.3-inch 5-megapixel (MP) IPS monitor has received FDA clearance for digital mammography and breast tomosynthesis. …
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FibriCheck, a DigitalHealth.London Accelerator alumnus company, announce their Food and Drug Administration (FDA) clearance and the commercial launch of their technology within the US. Their medically certified technology utilises consumer devices and redefines how…
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Hyperfine, a pioneering medical device company, has announced the FDA clearance of its latest software update for the Swoop system, the world’s first FDA-cleared portable magnetic resonance brain imaging device. This ninth-generation AI-powered software…
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