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. ...
Mason has more than 25 years of experience in the medical device industry and more than a decade of executive-level healthcare leadership expertise...
The new x-ray irradiator uses tomosynthesis-based 3D imaging and faster dose delivery to make targeted preclinical radiotherapy studies more accessible to research laboratories. ...
The company posted a strong first-quarter performance, supported by continued momentum in home healthcare, strategic acquisitions and operational efficiencies across its senior care platform...
The healthcare software provider delivered robust top-line growth during the quarter, with revenue rising 47 per cent year-on-year to $31.9 million...
The redesigned website expands clinical evidence, workflow guidance and access pathways for the Vivio System, an FDA-cleared non-invasive device used to measure elevated left ventricular end-diastolic pressure in outpatient settings. ...
The new patent expands protection around Spinal Resources’ variable-stiffness spinal fixation platform, strengthening its intellectual property position across the rod, implant system, and AI-enabled patient-specific design methodology. ...
Industry veteran to lead marketing strategy and strengthen commercial execution...
The patented technology describes methods for obtaining a patient’s bone density information...
