Aug. 13, 2026 — Aidoc has announced that the Centers for Medicare & Medicaid Services (CMS) has approved a New Technology Add-on Payment (NTAP) for the CARE Multi-Triage CT Body device1, providing a Medicare Fee For Service add-on payment for eligible inpatient use of the FDA-cleared AI technology in analyzing and triaging patient cases with a broad set of acute findings.

Aug.12, 2026 — Mendaera Inc. has announced results from a peer-reviewed study showing that its FDA-cleared Focalist system, which combines handheld robotics, real-time imaging and intelligent guidance software, achieved technical success in 60 of 61 ultrasound-guided percutaneous procedures with zero device-related adverse events.


Radiologists spend much of their day moving between different systems: One application to review images. Another to access clinical information. Another to launch AI tools. Another to dictate findings and finalize radiology reports.

Each step serves a purpose. But when systems are disconnected, the burden falls on the radiologist to pull information together, navigate multiple applications and manage the handoffs between them. That cognitive burden adds pressure to teams already managing rising imaging volumes, workforce shortages and increasingly complex cases. 


Aug. 6, 2026 — Proscia has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for Concentriq AP-Dx. The clearance includes compatibility with the Leica Aperio GT 450 DX slide scanner, cloud deployment, and a Predetermined Change Control Plan (PCCP). Concentriq AP-Dx is a digital pathology platform for primary diagnosis used by laboratories of all sizes. 

Aug. 13, 2026 — An updated clinical guideline from the American Society for Radiation Oncology (ASTRO) provides evidence-based recommendations on the use of radiation therapy to treat adult patients with pancreatic cancer. The guideline updates ASTRO’s 2019 recommendations to reflect recent clinical trials that provide growing evidence for radiation therapy in the resectable, locally advanced and metastatic settings.

Aug. 10, 2026 — Teledyne Technologies Inc. and Varex Imaging Corp. have jointly announced that they have entered into a definitive agreement under which Teledyne will acquire all of the outstanding common shares of Varex. The transaction was unanimously approved by the Boards of Directors of Teledyne and Varex.

Aug. 13, 2026 — Artera has announced the enrollment of the first patient in its DIRECT-AI registry study, marking the beginning of real-world prospective evidence generation for the first nationwide registry evaluating the clinical utility of an AI-powered prostate cancer test. The first patient was enrolled at The Urology Place, a leading independent urology practice in San Antonio, Texas, recognized for its commitment to advancing innovation in prostate cancer care.

Aug. 13, 2026 – Perimeter Medical Imaging AI recently announced that Intermountain Health, the largest nonprofit health system in the Mountain West region, has become the first health system in the U.S. to commercially deploy Perimeter's Claire OCT System, an FDA-approved imaging device that uses AI during breast cancer surgery to help surgeons see microscopic tissue structures — where cancer can be difficult to detect — in real-time, for margin assessment.

Aug.11, 2026 – Leica Biosystems has received multiple U.S. Food and Drug Administration (FDA) 510(k) clearances that strengthen its connected clinical digital pathology portfolio, including its AI-assisted quality control software. These advancements are designed to help pathology laboratories deliver high-quality digital images more consistently and efficiently to support timely, confident diagnoses for patients at a critical moment when case volumes, staffing pressures, and diagnostic complexity continue to increase.

Aug. 1, 2026 — Candelis recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for ImageGrid StreamVue, the company's next-generation enterprise imaging and diagnostic viewing platform.

StreamVue provides radiologists and physicians with fast, intuitive access to diagnostic-quality images across multiple imaging modalities while offering healthcare organizations unprecedented flexibility in deployment and integration.

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