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# Siemens Healthineers Angiography System Cleared
- URL: https://www.fdaweb.com/siemens-healthineers-angiography-system-cleared/
- Published: 2022-07-29T12:00:00.000Z
- Updated: 2026-09-14T17:54:04.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5152407

FDA has cleared a Siemens Healthineers 510(k) for the ARTIS icono ceiling, a ceiling-mounted angiography system designed for routine and advanced procedures in interventional radiology and cardiology. The device’s new rotational capabilities and simplified cabling of its C-arm permit cone beam CT data acquisitions in 2.5 seconds at the patient’s head and 4 seconds at the left and right sides of the body, according to the company. “This extremely short 3D spin time reduces motion artifacts and requires less contrast media,” it says.

The company says that Artis’ predefined case flows settings allow precise intraoperative guidance and excellent clinical outcomes with minimal user interaction, faster system positioning, and reduced patient radiation dose.