FDA clears tomosynthesis feature of Nanox digital radiography system

Israel-based Nano-X Imaging (Nanox) has received additional U.S. Food and Drug Administration (FDA) 510(k) clearance for the Nanox.ARC, an x-ray system incorporating advanced tomosynthesis technology to produce tomographic images for general use on adults.

These images may include the musculoskeletal system, pulmonary, intra-abdominal, and paranasal sinus indications.

The Nanox.ARC has a proprietary digital x-ray source. It utilizes advanced tomosynthesis technology with a cold cathode to create a more comprehensive sliced three-dimensional view of the body, enhancing visualization with multiple layers of images, and reducing the superimposition of structures that may be seen into dimensional x-rays, according to the company.

It has a smaller footprint than conventional stationary radiography systems, requires less power, and utilizes a matrix pattern that blurs out structural noise.

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