Applications Now Being Accepted for for Imaging for Impact Award
Cassling has opened applications for its 2026 Imaging for Impact Award, a national program recognizing imaging professionals and healthcare teams that improve patient outcomes and expand access to care. Submissions are accepted through April 1, 2026, and the award, now in its second year, highlights innovative projects such as mobile mammography and workforce recruitment. Last year’s winner, Children’s Health of Plano, was honored for making MRI procedures more accessible to hearing‑impaired patients. The initiative seeks to showcase best practices and strengthen the imaging community nationwide.
Lunit to Be Featured in 21 AI Imaging Studies on Breast Cancer, Lung Disease at ECR 2026
Lunit will showcase 21 AI imaging studies at the European Congress of Radiology 2026 in Vienna, including oral and poster presentations of its INSIGHT MMG, Scorecard and INSIGHT CXR solutions. A breast‑cancer risk‑assessment trial of 67,686 women showed risk scores...
FDA Grants 510(k) Clearance for Expanded Capabilities of MR Injection System
The U.S. Food and Drug Administration granted Bayer 510(k) clearance for its MEDRAD MRXperion injector, extending the device’s approved magnetic field compatibility to include 7‑Tesla MRI scanners. The clearance also adds Imaging Scanner Interface 2 (ISI2), enabling direct communication between...
MedDream to Present AWS-Powered Imaging Viewer at HIMSS
MedDream will demonstrate its cloud‑native, AI‑ready universal DICOM viewer, built on AWS HealthImaging, at HIMSS 2026 in Las Vegas. The solution leverages AWS’s HTJ2K transfer syntax to stream large imaging datasets quickly and securely. It supports radiology, cardiology, ophthalmology, dental...
Ultrasound Reporting Platform Gets FDA Approval
AS Software announced that its next‑generation ultrasound reporting platform, Asera, received 510(k) clearance from the U.S. Food and Drug Administration. The cloud‑based solution retains core reporting functions while delivering a redesigned user interface, streamlined workflows, and scalable architecture. Asera includes...
Researchers Use Dynamic Digital Radiography to Quantify Functional Outcomes After Total Shoulder Arthroplasty
Emory Healthcare researchers used Konica Minolta's Dynamic Digital Radiography (DDR) to compare anatomic and reverse total shoulder arthroplasty (aTSA and rTSA) in 71 shoulders versus 32 healthy controls. The DDR cine‑loop analysis showed that both procedures restored scapulohumeral rhythm (SHR)...
Multicenter Study Shows High Local Tumor Control After Resection with GammaTile in Newly Diagnosed Brain Metastases
GT Medical Technologies released Phase IV registry data showing that GammaTile brachytherapy, implanted at the time of surgical resection, achieved 92.3% local tumor control in newly diagnosed brain metastases after a median 12.4‑month follow‑up. The study of 51 patients reported a...
Targeted PET/CT Tracer Helps Rheumatoid Arthritis Patients
A new macrophage‑targeted PET/CT tracer (11C‑DPA‑713) can identify rheumatoid arthritis patients who will respond to anti‑TNF therapy within four weeks, far earlier than the traditional three‑to‑six‑month window. The study of 20 patients showed that standardized uptake values (SUVs) at baseline...
Positrigo Launches BrainPET Accelerator Program in U.S.
Positrigo, a Swiss developer of nuclear medical devices, has launched the BrainPET Accelerator Program in the United States, offering neurology practices a ready‑to‑operate brain PET solution. The program bundles a compact NeuroLF scanner, radiotracer logistics, regulatory assistance, reimbursement support, and...
FDA Clears Six Indications for Qure.ai's Chest X-Ray Reporting Tool
The FDA granted 510(k) Class II clearance to Qure.ai’s qXR-Detect, adding six new chest‑X‑ray detection indications. The tool now flags findings across lung, pleura, mediastinum/hila & heart, bone, hardware and other regions, expanding the company’s U.S. portfolio to 26 FDA clearances. The clearance...
