November 25, 2019 – Canon U.S.A., Inc. introduced the new CXDI-702C and CXDI-402C wireless detectors. These new detectors offer customers the superb quality and reliability, as well as the features and accessories, of the CXDI-710C, CXDI-810C and CXDI-410C wireless detectors. Both have received FDA 510(k) clearance.

November 25, 2019 — Researchers using magnetic resonance imaging (MRI) have found signs of damage that may be related to inflammation in the brains of obese adolescents, according to a study being presented next week at the annual meeting of the Radiological Society of North America (RSNA).

November 25, 2019 — Lunit announced the certification of CE mark for its most up-to-date chest X-ray analysis AI, Lunit INSIGHT CXR. The software provides analysis of chest x-ray images, detecting major findings that can lead to the most common lung diseases.

November 25, 2019 — Blackford, the centralized medical imaging platform, today announced that it had signed a multi-year agreement with IBM to integrate the Blackford Registration into IBM’s AI-ready workflow platform, Merge PACS.

November 25, 2019 — Zebra Medical Vision announced that its AI1 “all-in-one” bundle of artificial intelligence (AI) products will be available on the

November 25, 2019 — Connectivity in an area of the brain that regulates emotion may be altered in infants exposed to opioids while in utero, according to a new study being presented next week at the annual meeting of the Radiological Society of North America (RSNA).

November 25, 2019 — Embrace Neonatal MRI is a U.S. Food and Drug Administration (FDA) cleared and CE marked compact magnetic resononance imaging (MRI) system ergonomically designed to fit inside the neonatal intensive care unit (NICU). This point-of-care approach keeps critically ill infants safe in a temperature-controlled environment, eliminating the risk of transporting delicate newborns to an external MRI system.

November 25, 2019 — CurveBeam introduced the next level of weight-bearing computed tomography (CT) imaging, which will have the unique capability of scanning the hip and pelvis in weight bearing position, at RSNA 2019.

With the HiRise, musculoskeletal radiologists and orthopedic specialists will be able to assess alignment of the total leg in three dimensions. The HiRise is investigational only and is not available for sale in the United States.

November 22, 2019 — Carestream’s Dual-Energy imaging technology and its Focus 35C digital radiography (DR) detector with Image Suite Software have received 510(k) clearance from the U.S. Food and Drug Administration (FDA). Both technologies will be showcased at Carestream’s booth #7513 at the upcoming Radiological Society of North America annual conference.

November 22, 2019 — In September, the Food and Drug Administration (FDA) issued draft guidance titled “Safer Technologies Program for Medical Devices,” a voluntary program that is expected to significantly improve the safety of available treatments or diagnostic devices for diseases or conditions that are less serious than those eligible for the agency’s

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