• Osteopore secures European Union Medical Device Regulation (EU MDR) approval to supply its cutting-edge custom orthopaedic and cranial implants. • EU MDR approval unlocks opportunities to offer high-value, custom implants to Europe, in addition to off-the-shelf implants, introducing new revenue streams. • Regulatory clearance validates Osteopore’s orthopaedic and cranial products in Europe, strengthening the Company’s positioning in the market. • The European orthopaedic market is projected...
Advanced Machine Learning Tool Integrates with Shoulder Planning App to Personalize Surgical Predictions...
Strategic collaboration extends TOOsonix's reach into Poland, addressing skin diseases for a population of over 37 million....
New results from the VERIFI study show Immunovia's test accurately detects 77% of early-stage cases and maintains strong specificity across diverse high-risk groups—strengthening commercial launch plans for Q3 2025....
Innovative software enhances MRI scan quality, reduces scan times by up to 80%, and optimizes radiology workflows without requiring hardware upgrades. ...
Zimmer Biomet Secures FDA Clearance for Persona® Revision SoluTion™ Femur, Expanding Options for Metal-Sensitive Knee Implant Patients...
With cases of atrial fibrillation and other heart rhythm disorders rising rapidly, the European Heart Rhythm Association (EHRA) calls for greater awareness and early detection—starting with a simple pulse check on 1 March....
Noor to lead strategy, M&A, and innovation initiatives, including integration of Paragon 28 acquisition. ...
Collaboration brings clinical-grade magnetoencephalography (MEG) technology to consumers, launching first brain health center in London....
At ECR 2025, the two companies unveil the next phase of their research program, developing scalable urine filtration systems to reduce contrast media waste and promote circular sustainability in hospital radiology....
