Anatomage Inc. released an update to the Anatomage Cloud platform that allows medical and dental professionals to quickly send 3-D DICOM volumetric data to colleagues for one-click review. The updated version provides a U.S. Food and Drug Administration (FDA)-approved 3-D DICOM web viewer with new tools such as measurements, the ability to discuss cases with messaging, viewing of mesh file types such as STL and more.

NorthStar Medical Radioisotopes LLC announced completion of construction on its 20,000-square-foot molybdenum-99 (Mo-99) processing facility in Beloit, Wis., with equipment installation currently underway. Establishing this processing facility is part of NorthStar’s staged development and dual processing pathway approach to expanding current capacity and efficiencies in Mo-99 production.

Featuring dual detectors, the Instadose2 dosimeter addresses international requirements for independent deep [Hp(10)] and shallow [Hp(0.07)] measurements of both photon and beta radiation.

Koios Medical announced its second 510(k) clearance from the U.S. Food and Drug Administration (FDA).

GE Healthcare and Insightec announced U.S. Food and Drug Administration (FDA) approval and CE mark for Insightec’s Exablate Neuro compatible with the Signa Premier magnetic resonance imaging (MRI) system from GE Healthcare. The Exablate Neuro is a focused ultrasound platform for treating deep in the brain with no surgical incisions. MR imaging provides a comprehensive anatomical survey of the treatment area, patient-specific planning and real-time thermal monitoring throughout the treatment.