Nexus DRF Digital X-ray Imaging System

Nexus DRF Digital X-ray Imaging System is an FDA 510(k)-cleared medical device (K253103) manufactured by Varex Imaging Corporation. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 28, 2026. Regulation: 8.