Breakthrough Device Peer reviewed In development

InVision Precision Cirrhosis

Opportunistic screening for cirrhosis and steatotic liver disease — from the subcostal view captured during routine echocardiography.

ROC — CIRRHOSIS DETECTION 0.84 AUROC FPR 1.0 TPR

What it does.

Chronic liver disease affects more than 1.5 billion adults worldwide, and most cases are asymptomatic and undiagnosed. Early cirrhosis can present with symptoms — fatigue, weakness, poor appetite, leg and abdominal swelling — that mimic heart failure, so patients may be worked up for the wrong condition entirely.

During every standard echocardiographic exam, the subcostal view captures the liver alongside the heart. Cardiologists typically aren't trained to evaluate hepatic texture and quality, so this information goes unused. InVision Precision Cirrhosis applies deep learning to the subcostal echo view to opportunistically screen for cirrhosis and steatotic liver disease — no additional imaging, no additional patient time.

The underlying EchoNet-Liver pipeline was developed from over 1.5 million echocardiogram videos and validated against paired abdominal ultrasound and MRI studies at two large academic medical centers. The research was peer-reviewed in NEJM AI (2025). In November 2025, the FDA granted Breakthrough Device Designation to Precision Cirrhosis, providing an expedited pathway for regulatory review. A prospective multi-center validation trial is underway, funded by the American Heart Association.

1.5B
Adults worldwide affected by chronic liver disease
0.84
AUROC for detection of cirrhosis on held-out internal test set
1.6M
Echocardiogram videos used to develop the EchoNet-Liver model

Peer-reviewed research behind the product.

Built for your existing workflow.

Indication
Opportunistic screening for cirrhosis and steatotic liver disease
Input
Subcostal view echocardiogram videos
Output
Risk prediction for cirrhosis and steatotic liver disease
Regulatory
FDA Breakthrough Device Designation (Nov 2025)
Validation
Multi-center; paired abdominal ultrasound and MRI reference standards
Funding
AHA-funded prospective multi-center clinical trial underway