FDA clears Konica’s Regius

Article

Konica of Wayne, NJ, became the latest company to join the digital x-ray party when it received 510(k) clearance on June 19 from the Food and Drug Administration for Regius, an x-ray digitization system based on storage phosphor technology. Konica

Konica of Wayne, NJ, became the latest company to join the digital x-ray party when it received 510(k) clearance on June 19 from the Food and Drug Administration for Regius, an x-ray digitization system based on storage phosphor technology. Konica introduced Regius at last year’s Radiological Society of North America meeting as a system for conducting digital chest and abdomen studies (SCAN 11/26/97).

Although Regius is similar to computed radiography in that it is based on storage phosphor, unlike CR it does not require storage phosphor plates to be removed and taken to a separate reader. Images can be acquired and processed in 20 seconds and sent directly into a DICOM-based network. Konica has already installed over 20 Regius systems in Japan.

Newsletter

Stay at the forefront of radiology with the Diagnostic Imaging newsletter, delivering the latest news, clinical insights, and imaging advancements for today’s radiologists.

Recent Videos
Reducing Mammography Workload by Nearly 40 Percent? What a New Hybrid AI Study Reveals
 What New Research Reveals About Portable Low-Field MRI and Patients with Suspected Alzheimer’s Disease
Diagnostic Imaging's Weekly Scan: August 11 — August 17 (Video Version)
© 2025 MJH Life Sciences

All rights reserved.