EchoGo

By Ultromics
· UK
Ultromics — Automated stress echocardiography analysis; EchoGo Heart Failure holds FDA Breakthrough Device status.
Diagnostic
Cardiology
Production
FDA Cleared
Regulatory status
FDA Cleared
Deployment
Production
Clinical role
Adjunct (decision support)
Headquarters
UK
AI type
Diagnostic

Precise indication

Automated stress echocardiography analysis; EchoGo Heart Failure holds FDA Breakthrough Device status.

Regulatory status

Multiple FDA clearances, including Breakthrough Device status for EchoGo Heart Failure.

Clinical evidence

Vendor-supported

Vendor-published study summary.

Independent

Published study describing improved diagnostic accuracy of stress echocardiography across SIX named NHS hospitals — a relatively strong, multi-site deployment claim for this scan.

Real-world deployment

Multi-site NHS deployment (six named hospitals) with a published accuracy-improvement study.

Interoperability

European status

Editorial verdict

Limits and uncertainties

Confirm the independence of the cited study (author affiliations, funding) before presenting it as fully independent evidence.

Sources

https://www.ultromics.com/press-releases/left-ventricular-assessment-using-ultromics-ai-increases-the-diagnostic-accuracy-of-stress-echocardiography-in-six-nhs-hospitals

This profile is not medical advice or an endorsement. Hospitals should perform their own due diligence (regulatory compliance, GDPR, cybersecurity, integration, local clinical validation). How we evaluate

At a glance
Vendor
Ultromics
Headquarters
UK
AI type
Diagnostic
Specialty
Clinical role
Adjunct (decision support)
CE marking
Notified body
EU AI Act
Data hosting
Last verified
Reviewed by
How we evaluate

Every profile documents the precise indication, regulatory status, vendor-supported and independent evidence, real-world deployment, limits and dated sources.

A independent systematic review or prospective multicentre study · B at least one independent peer-reviewed study · C peer-reviewed, vendor-supported · D vendor claims only.

Read the methodology →

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Vendors, authors and clinicians can request a correction. Corrections are dated on the profile.