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Medical AR company

SentiAR

Developer of augmented and mixed reality visualisation for cardiac electrophysiology, including an FDA-cleared platform that renders real-time catheter data as a hands-free 3D hologram.

Source reviewed
Appears inSurgical planning
StageImplementationRegulatoryCommercialization
Structured overview

What this record covers

GeographyUnited States
ModalitiesAR, MR
MaturityCommercial
Last reviewed2026-08-24

Clinical areas and use cases

Specialties

CardiologyElectrophysiology

Use cases

VisualizationPlanning
Regulatory context

United States: the company states its CommandEP platform is FDA-cleared. Regulatory status is region- and date-specific.

This is source-linked metadata, not an AVRMD endorsement or medical recommendation.
Regulatory record

On the FDA's AR/VR device list (2)

As published by the FDA. Authorization is a regulatory decision, not evidence of clinical effectiveness. All AR/VR devices
Provenance

Primary source

SentiAR official websiteProducts, clinical focus, and FDA-cleared status summarised from the official site.
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