GE secures FDA 510(k) and CE Mark for Allia Moveo

GE HealthCare (GEHC) has secured 510(k) clearance from the U.S. Food and Drug Administration (FDA) and the European CE Mark for its image-guided platform Allia Moveo. GEHC unveiled the platform at RSNA 2025.

GE HealthCare's Allia Moveo.GE HealthCare's Allia Moveo.GEHC

The interventional procedures platform consists of a cable-free C-arm system and includes AI tools such as CleaRecon DL, which removes streak artifacts caused by blood flow in the arteries; Motion Freeze, which offsets involuntary respiratory motion artifacts to improve image clarity; and Metallic Artifact Reduction, which reveals anatomic details obscured by metal artifacts.

Allia Moveo has been installed at Hôpital Marie-Lannelongue in Le Plessis-Robinson, France, GEHC said.

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