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

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.

Investors have seemingly homed in on flat sales in the Watchman and electrophysiology segments of Boston’s cardio portfolio, prompting a stock fall.

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 ...

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.

With the wearables market continuing to boom, smart patches could become the next big focus area for tracking healthcare ...

GE HealthCare has gained simultaneous US Food and Drug Administration (FDA) clearance and a European CE mark for Allia Moveo, ...

Medtronic has reported three milestones in the US, expanding access to its MiniMed 780G insulin delivery system for ...

Cynosure Lutronic has announced CE Mark approval under the European MDR for its Mosaic 3D fractional resurfacing platform.