Biocomposites gains EU MDR certification for antibiotics carrier
Biocomposites’ STIMULAN bone infection management products have gained certification under the European Union’s Medical Device Regulation (EU MDR). The British medtech …
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Boston Scientific’s shares tumble 18% despite strong FY25 growth
Despite reporting revenue of $20bn in its fiscal year 2025 (FY25) and strong growth in Q4 2025, Boston Scientific’s shares …
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UK’s NICE greenlights Abbott’s CardioMEMS heart failure sensor
The UK’s National Institute for Health and Care Excellence (NICE) has recommended medtech giant Abbott’s heart failure sensor CardioMEMS. This means …
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Jupiter Endovascular completes SPIRARE II trial enrolment for Vertex system
Jupiter Endovascular has completed patient enrolment in the SPIRARE II pivotal clinical trial of its Vertex pulmonary embolectomy (PE) system, …
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Hologic’s Aptima assay secures FDA approval for HPV primary screening
Hologic has received the US Food and Drug Administration (FDA) approval for its Aptima HPV assay for use in clinician-collected …
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J.P. Morgan Healthcare Conference 2026 Report
The J. P. Morgan Healthcare Conference 2026 (JPM 2026) offers an early view of investor sentiment in the healthcare industry …
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GE HealthCare reports FY25 revenue of $20.6bn amid strong imaging demand
GE HealthCare has achieved revenues of $20.6bn in fiscal year 2025 (FY25) amid ongoing imaging demand and now expects earnings …
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MHRA outlines upcoming IVD submission shift for clinical trials
The Medicines and Healthcare products Regulatory Agency (MHRA) is formalising its review process around in vitro diagnostics (IVD) or companion …
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Medtronic set to acquire CathWorks for $585m
Medtronic has announced plans to exercise its option to acquire medical device company CathWorks, which is focused on transforming the …
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Endospan reports one-year TRIOMPHE study results for NEXUS system
Endospan has announced positive one-year results from the TRIOMPHE study evaluating its NEXUS aortic arch stent-graft system. The multi-centre, three-arm, prospective …
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FDA clears RevealDX’s AI lung nodule diagnostic
RevealDX has obtained US Food and Drug Administration (FDA) clearance for RevealAI-Lung, an artificial intelligence (AI)-based software for lung nodule …
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Artivion’s aortic stents boost post-surgical outcomes in interventional studies
Artivion has debuted long-term clinical data on two of its cardiac stent products, revealing each’s solution’s potential to offer extended …
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GE HealthCare gains US-EU approval for Allia Moveo imaging system
GE HealthCare has gained simultaneous US Food and Drug Administration (FDA) clearance and a European CE mark for Allia Moveo, …
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Quest launches flow cytometry MRD test for myeloma
Quest Diagnostics has introduced a new flow cytometry measurable residual disease (MRD) blood test for myeloma, a cancer arising from …
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Medtronic achieves three milestones for MiniMed 780G system in US
Medtronic has reported three milestones in the US, expanding access to its MiniMed 780G insulin delivery system for individuals with …
