VISIE Inc., previously known as Advanced Scanners, has announced the successful demonstration of Continuous Anatomic Auto Tracking (CAAT) for robotic-assisted total knee arthroplasty (RA-TKA) at their headquarters in Austin, Texas.
Paragonix Technologies has announced the first paediatric use of its BAROguard Donor Lung Preservation System. The transplantation was performed at UF Shands Children’s Hospital in Gainesville, Florida, USA.
Paragon 28, Inc. has launched the Phantom® Fibula Nail System, offering a less invasive approach to fibular fracture treatment in ankle injuries. The system, designed to provide an alternative to traditional plate and screw fixation, purportedly addresses some of the complications associated with external fixation methods.
GE HealthCare has introduced the Venue Sprint, a new tablet-based ultrasound device, alongside enhancements to its existing Venue family of point-of-care ultrasound (POCUS) systems. The launch aims to address the growing demand for portable, high-quality imaging solutions in various clinical settings.
GE HealthCare has introduced the Versana Premier, a new multi-purpose ultrasound system designed to meet the diverse needs of healthcare professionals across various clinical specialties. The system, which forms part of the Versana ultrasound family, incorporates artificial intelligence (AI) and automated productivity tools to streamline workflow and improve clinical efficiency.
Catalyst OrthoScience, a medical technology company specialising in shoulder arthroplasty, has announced FDA 510(k) clearance for its Catalyst Fracture Shoulder System. The system, designed for reverse shoulder arthroplasty in cases of proximal humeral fractures (PHFs), aims to tackle the complexities associated with tuberosity fixation and healing.
bioAffinity Technologies’ Vice President of Diagnostics, Dr Jennifer Rebeles, has contributed to a new set of guidelines for flow cytometry testing on rare matrix samples. The peer-reviewed paper, published in Cytometry Part B: Clinical Cytometry, addresses the challenges and considerations in validating assays with unique sample types.
AtriCure has announced regulatory approval for the sale of its EnCompass® Clamp in CE-marked countries within the European Union. This development follows the device’s FDA 510(K) clearance and subsequent launch in the United States in 2022.
FUJIFILM Healthcare Europe has announced that its high-end ultrasound system, the ARIETTA 750 FF ENDO, is now compatible with FUJIFILM’s ultrasound endoscopes and endobronchial ultrasound scope. This advancement allows clinicians to fully leverage FUJIFILM’s endoscopic technology during diagnostic and therapeutic procedures.
Vitestro, a Dutch medical robotics firm, has announced that its autonomous blood drawing device has received CE marking, making it the first such device to be approved for commercial use in the European Union. This milestone, achieved in July 2024, signifies the device’s compliance with the European Medical Device Regulation (MDR) standards for safety and […]
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