There is a significant unmet need for effective brain monitoring across various healthcare settings — including emergency departments, intensive care units, outpatient clinics and home environments — due in large part to the persisting…
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What You Should Know:
– Eko Health, a leader in AI-powered early detection of heart and lung diseases, announced today a successful Series D financing round of $41 million.
– This funding, led by ARTIS Ventures,…
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What You Should Know:
– Implicity, a leader in remote patient monitoring and cardiac data management, has received FDA 510(k) clearance for SignalHF1, a groundbreaking new algorithm within their remote monitoring solution.
– SignalHF1 algorithm empowers…
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The demand for home sleep apnea testing (HSAT) devices is escalating, particularly in the context of the coronavirus 2019 (COVID-19) pandemic. The absence of standardized development and verification procedures poses a significant challenge. This…
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What You Should Know:
– RapidAI, a global leader in AI-powered solutions for combating life-threatening vascular diseases, announced today the FDA 510(k) clearance for its innovative AngioFlow™ by RapidAI solution.
– The technology empowers interventional care…
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2023 was a banner year for MedTech, especially in terms of technological innovations. Incidentally, it also witnessed the largest ever number of FDA approvals on novel medical devices in a single year. This list…
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What You Should Know:
– GE HealthCare has received FDA 510(k) clearance for its innovative Portrait VSM vital signs monitor. This portable device promises to revolutionize patient care by offering clinicians a more efficient and…
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Baby tech company Owlet and telehealth staffing and services company Wheel announced they are partnering to allow Wheel’s clinicians to prescribe caregivers Owlet’s medical pulse oximetry wire-free sock for infants. Owlet’s BabySat, which received FDA…
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What You Should Know:
– Scopio Labs, a leader in digital cell morphology, has achieved a major breakthrough with FDA De Novo clearance for its Full-Field Bone Marrow Aspirate (FF-BMA) Application.
– The FDA clearance marks…
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Current solutions for remote health monitoring can be seen as invasive by patients and mostly do single variant intermittent tracking. FDA clearance brings one of Europe’s most advanced real-time continuous remote monitoring systems to…
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