Rayence Universal Digital Radiography System Receives FDA Clearance

May 5, 2015 — Rayence Inc. announced that the RU-3000 Digital Universal Radiography System has received 510(k) clearance from the U.S. Food and Drug Administration (FDA). The RU-3000 is the first U-arm system to be marketed by Rayence in the United States. Its small footprint and compact design allows for easy installation, and its dual telescoping arm movement permits installation in settings having ceiling heights of just 8 feet.

The Rayence RU-3000 has fully motorized movements for source to image receptor distance (SID), arm rotation, height and detector angle; movements can be automatically programmed to user-specific radiographic positions by either the intuitive touchscreen located on the tube head or by a handheld remote control. The system comes with a high-quality Rayence 17x17-inch cesium detector, which is coupled with Rayence’s XmaruView workstation. Complemented by a durable bucky design with an easily removable grid, patient safety anti-collision sensors and an available mobile table, the RU-3000 is well-suited for all imaging environments, especially orthopedics, imaging centers and urgent care.

For more information: www.rayenceusa.com