South Korea-based MOPIC has introduced an autostereoscopic 3D display aimed at endoscopic and microscope imaging applications ...

VentureMed has raised $28m to accelerate the commercial adoption and expand indications for its FLEX Vessel Preparation (FLEX ...

Roche has obtained CE mark approval for its fully automated immunoassay, Elecsys Dengue Ag test, intended for diagnosing ...

Elucid has launched PlaqueIQ, an AI-based image analysis software that quantifies plaque build-up to evaluate a patient’s ...

The FDA has granted breakthrough device designation to Augurex’s SPINEstat 14-3-3eta Autoantibody Multiplex Immunoassay Test.

AtriCure has treated the first subject in the randomised Box Lesion Creation with Left Atrial Appendage Exclusion to Reduce ...

Co-Dx has signed a definitive agreement with Arabian Eagle Manufacturing to create a joint venture (JV) for PCR platform ...

As healthcare systems increasingly turn to personalised approaches, Belgian company Materialise is accelerating efforts to ...

The US Food and Drug Administration (FDA) has hit Philips with a warning letter after quality control shortcomings were uncovered at three of its medical device manufacturing sites.

Pearsanta, a subsidiary of Aditxt, has commenced enrolment in a clinical trial to assess the blood-based Mitomic ...

Alife Health’s AI-powered selection tool, Embryo Predict, has received the CE Mark certification in compliance with the ...

Edwards Lifesciences’ transcatheter aortic valve replacement (TAVR) system has demonstrated positive results in a long-term ...