Varex Imaging Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Varex Imaging Corporation - FDA 510(k) Cleared Devices
Recent clearances: Nexus DRF Digital X-ray Imaging System, Nexus DR Digital X-Ray Imaging System (with vSharp), Nexus DR Digital X-ray Imaging System
7
Total
7
Cleared
0
Denied
Varex Imaging Corporation has 7 FDA 510(k) cleared medical devices. Based in Liverpool, US.
Latest FDA clearance: May 2026. Active since 2017. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Varex Imaging Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Varex Imaging Corporation
7 devices
Cleared
May 29, 2026
Nexus DRF Digital X-ray Imaging System
Radiology
247d
Cleared
Dec 20, 2019
Nexus DR Digital X-Ray Imaging System (with vSharp)
Radiology
25d
Cleared
Mar 08, 2019
Nexus DR Digital X-ray Imaging System
Radiology
38d
Cleared
Dec 07, 2018
Nexus DR Digital X-ray Imaging System with stitching
Radiology
18d
Cleared
Jul 03, 2018
XRpad2 4343 HWC-M Flat Panel Detector
Radiology
22d
Cleared
Oct 24, 2017
Nexus DR Digital X-ray Imaging System (with PaxScan 4343RC and PaxScan 4343Rv3)
Radiology
28d
Cleared
May 17, 2017
Nexus DR Digital X-ray Imaging System
Radiology
29d