A fault in J&J MedTech’s CEREPAK detachable coils, used in intracranial aneurysm embolisation procedures, has been associated ...

With financial support from Medtronic, the university’s new hub is intended to drive innovation in the medical device space.

Wearables in healthcare must advance to a stage where they provide actionable insights in addition to datapoints.

The US FDA has granted 510(k) clearance for Eyas Medical Imaging’ Ascent3T neonatal MRI system, a device engineered ...

GE HealthCare has announced an AI-enabled foetal ultrasound collaboration with Diagnoly, a deeptech company known for ...

Hologic has received the US Food and Drug Administration (FDA) approval for its Aptima HPV assay for use in clinician-collected primary screening, further expanding its cervical health portfolio.

Jupiter Endovascular has completed patient enrolment in the SPIRARE II pivotal clinical trial of its Vertex pulmonary embolectomy (PE) system.

GE HealthCare’s imaging vertical was the most significant in terms of overall revenue, with revenue of $9.25bn reflecting a 4 ...

Medtronic has announced plans to exercise its option to acquire medical device company CathWorks, which is focused on ...

Abbott's CardioMEMS sensor will now be available to patients with chronic heart failure through the NHS, as per NICE's ...

The Medicines and Healthcare products Regulatory Agency (MHRA) is formalising its review process around in vitro diagnostics (IVD) or companion diagnostics (CDx) used in clinical trials, with failure ...

Endospan has announced positive one-year results from the TRIOMPHE study evaluating its NEXUS aortic arch stent-graft system.