Zimmer Biomet reports 2025 revenue growth yet tempers 2026 outlook
Zimmer Biomet has achieved revenue of $8.23bn in full year 2025 off the back of continued strong demand across its …
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UK government champions healthtech through new NHS access programme
The UK government has set out to improve access to healthcare technology within the National Health Service (NHS) through the …
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BD shares fall by 3% after lowering FY26 profit outlook
Becton Dickinson and Company (BD) has trimmed its fiscal year 2026 (FY26) profit outlook to account for the spin-off of …
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RWD and RWE are rewriting how we design and run trials
Traditional randomized controlled trials (RCTs) have long been the gold standard for testing new therapies, but they are increasingly strained …
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GE HealthCare introduces ReadyFix in US to improve patient care
GE HealthCare has announced the US launch of ReadyFix, a remote fleet management solution designed to help healthcare systems optimise …
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TransMedics receives IDE approval from FDA for OCS Heart trial
TransMedics Group has received full and unconditional investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) …
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FDA clears Median Technologies’ lung nodule evaluation software
The US Food and Drug Administration (FDA) has cleared a lung cancer detection tool on Median Technologies’ eyonis, a suite …
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Medtronic ordered to pay $382m in anticompetitive surgical device lawsuit
A California court has ordered Medtronic pay surgical device rival Applied Medical almost $382m in damages after determining that the …
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Sonorous receives FDA breakthrough designation for BosSTENT device
Sonorous Neurovascular has received breakthrough device designation from the US Food and Drug Administration (FDA) for its braided, self-expanding cerebral …
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Abbott reports positive VERITAS study results for AFib
Abbott has reported positive early data from the VERITAS study, evaluating its investigational Amulet 360 left atrial appendage (LAA) occluder, …
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FDA classifies J&J MedTech’s CEREPAK recall as Class I following patient death
The US Food and Drug Administration (FDA) has classified the recall of Johnson & Johnson (J&J) MedTech’s CEREPAK Detachable Coil …
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University of Galway opens medtech prototype hub under Medtronic partnership
Ireland’s University of Galway has a launched a new medical device prototype hub, representing the latest milestone in its ongoing …
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Wearables’ future in healthcare likely to hinge on actionable insights
The days of wearables collecting data and merely providing these insights back to users are numbered, with the inclusion of …
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GE HealthCare and Diagnoly integrate AI solutions for foetal ultrasound
GE HealthCare has announced an AI-enabled foetal ultrasound collaboration with Diagnoly, a deeptech company known for prenatal screening. The agreement aims …
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FDA grants clearance for Eyas Medical Imaging’s neonatal MRI system
The US Food and Drug Administration (FDA) has granted 510(k) clearance for Eyas Medical Imaging’s Ascent³ᵀ neonatal magnetic resonance imaging …
