Europe

GammaPod Introduces Single-Session High-Dose Stereotactic Radiotherapy for Breast Cancer in Europe

A new technology marks a turning point in the treatment of early-stage breast cancer ...

Telix's Illuccix PSMA-PET Imaging Agent Approved in France

New approval provides French hospitals and clinics with access to a proven PSMA-PET imaging agent ...

Europe: Sanoculis Earns CE Mark for MINT® Device in Glaucoma Treatment

The minimally invasive MINT® procedure offers a novel, sutureless solution for managing intraocular pressure in glaucoma patients....

Eko Health Launches AI Stethoscope Platform in the UK

Clinicians across the United Kingdom can now access Eko's advanced digital stethoscopes, auscultation accessories, and AI-supported tools via EkoHealth.com and Amazon UK....

Turbett Surgical Secures FDA 510(k) Clearance for Enhanced Instrument Pod Portfolio

New TS1200 model supports up to 300 lbs, offering hospitals a more efficient, scalable solution for surgical instrument transport and storage....

Inbiome Shatters Diagnostic Delays: IVDR-Certified Platform IDs Bacteria in 5 Hours Across EU Hospitals

Hours, Not Days: EU Approval Accelerates 5-Hour Pathogen ID for Critical Cases. Molecular Fingerprinting: AI-Powered ‘DNA Barcode’ Spots 200+ Species, Including Uncultivable Pathogens. Hospital Laboratories Across Europe Now Have Immediate Access To a Fully Certified, Untargeted Molecular Diagnostics Platform. ...

ZEISS Receives FDA Clearance for INTRABEAM 700 – Germany

Robotic-Assisted Platform Enhances Intraoperative Radiation Therapy for Neuro-Oncology and Breast Cancer Treatments...

Orexo Reports Positive Data for Powder-Based Intranasal Vaccine with AmorphOX® Technology – Sweden

The collaboration is in line with Orexo's strategy to broaden the use of its powder-based drug delivery technology, AmorphOX®....

Sectra Expands Fully Managed AI Offering to Pathology with New Paige.AI Partnership – Sweden

Collaboration Enhances Cancer Diagnostics by Integrating Advanced AI into Unified Imaging Workflows...

Osteopore secures European approval for custom orthopaedic and cranial implants

• 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...