What You Should Know:
– Click Therapeutics, Inc. (“Click”), a leader in the rapidly evolving field of prescription medical treatments, encompassing both prescription digital therapeutics (PDTs) and software-enhanced drug™ therapies has received FDA marketing authorization…
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Glucose monitoring specialist Dexcom announced it received FDA clearance for its G7 15 Day continuous glucose monitoring (CGM) system for people 18 and older with type 1, type 2 and gestational diabetes. G7 15 Day,…
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Remote patient monitoring startup Sibel Health closed a $30 million Series C funding round on Thursday, bringing its total funding amount to $63 million.
The company — founded in 2018 as a spinout of Northwestern…
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Patient monitoring company Sibel Health, a spin-out of Northwestern University, closed a $30 million Series C equity financing round and received its seventh FDA clearance. Steele Foundation for Hope led the round with participation by…
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EpiWatch, the Apple Watch-based epilepsy management company spun out from Johns Hopkins, announced it received FDA 510(k) clearance for its continuous seizure monitor platform that utilizes the popular wearable to detect and alert for…
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FDA Clears Siemens Healthineers’ Innovative Technology
Siemens Healthineers has achieved a significant milestone with FDA clearance for its groundbreaking Naeotom Alpha class of photon-counting computed tomography (CT) scanners. This revolutionary technology represents a major advancement…
Google has received FDA clearance for its loss of pulse detection feature available on Pixel Watch 3. The loss of pulse detection technology checks for an individual’s pulse. Once it detects signs of a loss…
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What You Should Know:
– Google today announced a major advancement in wearable technology with the FDA clearance of its Loss of Pulse Detection feature for the Pixel Watch 3.
– The feature can detect when…
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What You Should Know:
– Ezra, a innovator in AI-driven cancer screening, today announced that its advanced Ezra Flash AI model has received 510(k) clearance from the U.S. Food and Drug Administration (FDA).
– The FDA…
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Aidoc has received FDA clearance for a computer-aided rib fracture triage offering (CADt AI) powered by a foundation model.CADt AI is an image processing prescription software designed to aid in prioritization and triage of…
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