Jan. 15, 2013 – Viztek, the advanced digital imaging solution provider, has received United States Federal Food and Drug Administration (FDA) 510k clearance for the ViZion + DR line of panels. This new family of products includes multiple panels in tethered, wireless and fixed configurations offering high quality images at quick speeds, while remaining at a competitive price point. Unlike many competing products, the panels have an ease of adaptability and require no generator interface.
Viztek President Joe Cermin notes, “Our team is very excited to bring this new technology to market. The panels give Viztek the strong advantage of sales exclusivity with an important new line of products.”
The ViZion + DR panel product line has an extremely versatile range of applications, including new x-ray rooms, retrofit rooms, and mobile implementations. The fixed panels will be available in Viztek’s Straight Arm and U-Arm configurations.
For more information: www.viztek.net
March 25, 2026 
