Intuitive’s shares fall 8% after tempering 2026 procedural growth outlook
Intuitive reported strong Q3 growth, yet its shares fell by almost 8% after revealing a tempered robotic surgery procedural growth …
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AMA weighs in on FDA’s regulatory proposal for GenAI-based medtech
The American Medical Association (AMA) has responded to the US Food and Drug Administration’s (FDA) call for feedback on its …
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Enabling surgical precision: Force feedback and coreless BLDC motors in robotic surgery
Matthew Dean, head of medical business unit, maxon UK & Ireland, explains how force feedback optimises control in robotic surgery, …
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IceCure enrols initial patients for ProSense cryoablation trial in US
IceCure Medical has enrolled its first two patients across two clinical centres in the US for the ChoICE study, assessing …
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Abbott secures CE Mark for Cologuard Plus cancer test
Abbott has secured CE Mark approval under the EU’s In Vitro Diagnostic Medical Devices Regulation (IVDR) for its Cologuard Plus …
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Medtronic’s next-gen pacemaker portfolio secures CE mark
Medtronic’s Vitalis portfolio of next-generation pacemakers, each of which has been engineered for conduction system pacing (CSP) therapy, has received …
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Formacoat continues to impress with coating technology HydroMark™
CHASKA, MINN. — Formacoat, a medical device coating services provider with nearly 25 years of experience, is expanding beyond coating …
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WHO grants bioMérieux’s Ebola panel emergency listing amid ongoing Bundibugyo outbreak
The World Health Organization (WHO) has granted bioMérieux’s panel for detecting the Bundibugyo (BVD) virus an emergency use listing (EUL), …
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UK government urged to scrap 20% VAT on defibrillators ahead of Autumn Budget
Ahead of the UK Autumn Budget on 28 October, 57 British parliamentarians have signed an open letter urging the chancellor …
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Designing for clarity before designing solutions
Lucy Baldwin, head of research and strategy, and Oliver North, head of engineering at Ensera Design, reflect on the key …
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Masimo’s vitals monitor scoops FDA clearance for AFib detection
The US Food and Drug Administration (FDA) has granted Masimo clearance for atrial fibrillation (AFib) detection via Radius VSM, further …
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FDA clears Sequel Med Tech’s twiist system for type 2 diabetes
The US Food and Drug Administration (FDA) has cleared Sequel Med Tech’s twiist automated insulin delivery (AID) system for adults …
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USC initiates trial of blood test for breast cancer
USC Norris Comprehensive Cancer Center, part of Keck Medicine of USC, has initiated a Phase I clinical trial to determine …
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Sirona Medical reels in $40m for cloud-based radiology platform scaleup
Sirona Medical has raised $40m, setting the US company up with proceeds to scale its artificial intelligence (AI)-based cloud-native radiology …
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Edwards’ SAPIEN M3 delivery system linked to patient death in FDA alert
The US Food and Drug Administration (FDA) has conveyed a ‘potentially high-risk’ issue affecting certain mitral valve delivery systems marketed …
