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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What You Should Know:
– AliveCor, the global leader in AI-powered cardiology, today announced that the American Medical Association (AMA) has granted new Category III Current Procedural Terminology (CPT) codes that are applicable to the company’s…
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What You Should Know: – Philips IntelliSite Pathology 5.1 has received 510(k) clearance from the FDA, solidifying its position as the most widely deployed digital pathology solution for primary diagnosis globally. – With over…
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Introduction
Clarius Mobile Health has recently announced that it has obtained U.S. Food and Drug Administration (FDA) clearance for its latest innovation, the Clarius OB AI fetal biometric measurement tool. This development marks a significant…
