GE HealthCare’s SOFIE deal deepens a complicated relationship with Lantheus
GE HealthCare’s planned $945m acquisition of SOFIE Biosciences has largely been read as a move to protect supply for Flyrcado, …
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FDA grants breakthrough device status to Teleflex’s coronary scaffold
Teleflex has received breakthrough device designation from the US Food and Drug Administration (FDA) for its Freesolve resorbable magnesium scaffold …
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Medtronic reports real-world findings for cardiac ablation systems
Medtronic has reported positive real-world registry findings for its cardiac ablation technologies in patients treated for atrial fibrillation (AFib) and …
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EQT to buy diagnostics player Qiagen for €9.6bn
EQT Private Equity has agreed to acquire German-Dutch molecular testing company Qiagen for €9.6bn ($10.7bn), reflecting the public market’s increasing …
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ESMO26: Lunit SCOPE studies highlight AI-based pathology benefit
Data from five studies involving Lunit’s SCOPE platform have demonstrated how artificial intelligence (AI)-based quantitative pathology can support research across …
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St Luke’s deploys hellocare.ai platform across Idaho sites in US
St Luke's Health System has selected technology supplier hellocare.ai to implement AI-assisted virtual care programmes across its inpatient facilities and …
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UK government confirms indefinite EU CE mark recognition
Medical equipment bearing a European CE mark will now be accepted on the British market indefinitely, meaning patients will retain …
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Edwards secures FDA approval for tricuspid valve repair system
The US Food and Drug Administration (FDA) has approved Edwards Lifesciences’ tricuspid valve repair system, PASCAL Precision. The transcatheter medical device …
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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 …
