Denver-based Matrix Analytics announced the company's rebrand to Eon. The rebrand marks the expansion of Eon's offerings beyond LungDirect to a suite of software solutions that will help improve the treatment of complex conditions of any kind. LungDirect, which will be rebranded to EonDirect, is the first and only cloud-based software application for lung cancer screening and incidental nodule management that integrates seamlessly with hospital electronic medical records (EMRs), according to Eon.

Accuray Inc. signed a multi-system, multi-hospital agreement with Mercy for the acquisition of Accuray Radixact and CyberKnife M6 Systems to expand access to advanced, life-saving technology for more cancer patients. The next-generation systems will replace existing Accuray devices as well as competitive conventional linear accelerators. The order was entered into backlog during the company's fourth fiscal quarter which ends June 30, 2018.

Having breast cancer placed a significantly greater financial strain on black women than white women, according to a study by researchers at the University of North Carolina Lineberger Comprehensive Cancer Center.

May 15, 2018 — U.S. First Lady Melania Trump underwent an interventional radiology embolization procedure to treat a benign kidney condition, according to a statement from the White House Press Office.

The White House said the procedure was successful and there were no complications. Mrs. Trump is at Walter Reed National Military Medical Center in Bethesda, Md., and she will likely remain in the hospital for the duration of the week.  

UKRCO

UKRCO is a co-hosted annual event organised on behalf of the British Institute of Radiology, the Society and College of Radiographers and the Institute of Physics and Engineering in Medicine.

On May 30, 2018, the American College of Radiology (ACR) Data Science Institute (DSI) and the Society for Imaging Informatics in Medicine (SIIM) will hold the Spring 2018 Data Science Summit: Economics of Artificial Intelligence (AI) in Health Care. The summit will be hosted at the SIIM 2018 Annual Meeting, May 31-June 2 in National Harbor, Md.

May 15, 2018 — Medic Vision Imaging Solutions Ltd. announced that the U.S. Food and Drug Administration (FDA) has cleared its latest product, iQMR (intelligent Quick MR).

FDA's MQSA Accreditation Bodies Approved for Tomosynthesis Accreditation

On April 9, 2018, the U.S. Food and Drug Administration (FDA) announced that all four of its Mammography Quality Standards Act (MQSA) accrediting bodies are approved to accredit digital breast tomosynthesis (DBT) systems. This includes the states of Arkansas, Iowa and Texas, and the American College of Radiology (ACR).

CurveBeam announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its LineUp Multi-extremity weight bearing computed tomography (CT) system.

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