The company will present Proliv Rx, its FDA-approved physician-directed neuromodulation therapy for adults with major depressive disorder who have not responded adequately to antidepressant medication. ...
The new technology division will serve as Mopec Group’s innovation hub, supporting digital tools that improve workflow efficiency, documentation and integration across the pathology continuum. ...
The recognition places Caracal’s nitrile examination glove within a vetted category of medical products meeting sustainability and safer chemical criteria for healthcare procurement. ...
The FDA marketing authorisation establishes a new Class II device category for Aurie’s automated reusable no-touch intermittent urinary catheter system, with launch planned in Veterans Health Administration spinal cord injury hospitals later this year. ...
The FDA 510(k) clearance advances Biozen’s BP1000, a handheld fingertip device designed to deliver clinically validated spot blood pressure measurements without an arm cuff or per-user calibration. ...
The event highlighted healthcare AI’s shift from experimentation to real-world deployment, with discussions on accountability, governance, workforce readiness and exhibitor solutions including Heidi and AITRICS-VC....
The approval allows Microsure to begin clinical use of its MUSA-3 microsurgical robotics system in Europe, while the appointment of Alex Joseph as CEO signals a shift from product development toward evidence generation, hospital adoption, and commercial execution. ...
The agreement supports Dentsply Sirona’s focus on disciplined distribution expansion, customer centricity, and localised commercial execution through established partners...
As COO, Testa’s responsibilities will span global operations, and he will oversee Confluent’s operations, supply chain, and global product development...
Funding to accelerate development of real-time imaging solutions aimed at improving surgical precision and patient outcomes...
