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# FDA Clears 2 Siemens Digital Radiography Devices
- URL: https://www.fdaweb.com/fda-clears-2-siemens-digital-radiography-devices/
- Published: 2021-01-21T12:00:00.000Z
- Updated: 2026-09-14T16:43:41.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148502

FDA has cleared a Siemens Healthineers 510(k) for the Multix Impact C ceiling-mounted digital radiography (DR) system as well as the Multix Impact VA20, a new version of the established floor-mounted parent DR system. Both devices feature intuitive operating systems, versatile wireless detectors, motorized tube heads, and a free-floating, flat tabletop for easier patient access. “With the X-ray tube’s touch user interface, the radiologic technologist can remain by the patient’s side for longer periods,” the company says.

The devices also use the company’s “myExam companion” user interface to provide proactive guidance to help technologists of any skill level navigate a radiography procedure, Siemens says. “With myExam Companion’s camera-based Smart Virtual Ortho feature, the technologist can set the field of view and adjust exposure parameters on the touchscreen using a live camera image of the patient, so long-leg and full-spine examinations can be set up and performed more easily,” it says.