FDA-cleared AI for echocardiography

A decade of research.
Built for every echo lab.

InVision delivers clinically-validated AI for the most common cardiac imaging exam in the world — streamlining interpretation, standardizing measurements, and surfacing disease that today goes undiagnosed.

Peer-reviewed in
Nature Nature Medicine Circulation JAMA Cardiology NEJM AI
Featured in
TCTMD Healio American Heart Association Cedars-Sinai Newsroom
32M
Echocardiograms performed in the US each year
10+
Years of academic research underpinning our models
3
Publications in Nature, including the first RCT of AI in cardiology
2
FDA-cleared algorithms, with an active clinical pipeline

Echo AI that earns its place on the enterprise roadmap.

“We wanted a partner with real evidence — not a pilot in search of a publication. InVision arrived with the Nature paper, the FDA clearance, and a deployment plan. That's a different conversation.” — Director, Cardiovascular Service Line
01

Reimbursement is live, not hypothetical

CPT Category III code 0932T (effective January 1, 2025) supports AI-assisted echocardiographic evaluation for patients with heart failure symptoms — providing a direct reimbursement path for Precision Cardiac Amyloid, not a budget ask that lives on indefinitely.

CMS · AMA-adopted · Effective 01.01.2025
02

Measurable workflow gains

Echo interpretation consumes over an hour of physician and technician time per exam. Precision LVEF has been shown in a blinded, randomized trial to reduce sonographer and cardiologist effort while improving measurement consistency.

Published in Nature (He et al., 2023)
03

Regulatory-grade from day one

FDA 510(k) clearance for both Precision LVEF and Precision Cardiac Amyloid. Cardiac Amyloid was previously granted Breakthrough Device Designation and enrolled in the FDA's Total Product Lifecycle Advisory Program (TAP).

FDA 510(k) · Breakthrough Device · TAP
04

Integrates with what you already own

Post-processing analysis of standard DICOM echo studies. No new hardware, no new scanners, no disruption to the cardiology workflow — deploys alongside your existing PACS, Epic EHR, and structured reporting platforms.

DICOM-native · PACS-compatible · Epic-compatible · SaMD
05

Surface the diseases you're missing

Cardiac amyloidosis is rare, under-diagnosed, and now treatable. Our algorithms screen every routine echo at zero marginal clinician burden — turning your existing imaging volume into a population-health instrument.

Rare disease detection · Heart failure · Cardiomyopathy
06

A roadmap, not a single product

LVEF and Cardiac Amyloid are live. Precision Cirrhosis holds Breakthrough Device designation, and Precision Reporting — powered by our Nature-published foundation model — is in active development. A single deployment path that grows across your cardiovascular service line.

Platform · Multi-indication · Future-proofed

One integration. A growing suite of cleared algorithms.

FDA 510(k) Cleared Prospective RCT

InVision Precision LVEF

Automated evaluation of left ventricular ejection fraction from standard echocardiographic DICOM images. The only AI-Echo product to undergo a blinded, randomized prospective clinical trial — published in Nature, demonstrating time savings and improved clinical precision.

InputDICOM echo
OutputEF, chamber metrics
EvidenceNature 2023
Learn more about Precision LVEF
58.3 % EF — NORMAL
FDA 510(k) Cleared Breakthrough Device FDA TAP Enrolled CPT 0932T

InVision Precision Cardiac Amyloid

AI screening for cardiac amyloidosis from apical-4-chamber and parasternal-long-axis echocardiographic views. Developed in collaboration with Alexion, AstraZeneca Rare Disease, to accelerate early detection of a life-threatening and routinely missed condition.

IndicationCardiac amyloidosis
Views requiredA4C + PLAX
EvidenceJAMA Cardiology 2022
Learn more about Precision Cardiac Amyloid
HIGH RISK LOW HIGH STUDY #2410
Breakthrough Device Peer reviewed In development

InVision Precision Cirrhosis

Opportunistic screening for cirrhosis and steatotic liver disease directly from the subcostal view already captured during routine echocardiography. Built on EchoNet-Liver — a deep learning pipeline developed from over 1.5 million echocardiogram videos and validated against paired abdominal ultrasound and MRI across two large academic medical centers.

IndicationCirrhosis · SLD
View requiredSubcostal
EvidenceNEJM AI 2025
Learn more about Precision Cirrhosis
ROC — CIRRHOSIS DETECTION 0.84 AUROC FPR 1.0 TPR
Foundation Model Nature 2025 JACC 2025 In development

InVision Precision Reporting

Automated, structured echocardiographic reports built on two complementary open-source foundation models. EchoPrime (Nature, 2025) — a multi-view vision-language model trained on over 12 million video-report pairs — delivers holistic clinical interpretation across 23 diverse benchmarks of cardiac form and function, validated in five international health systems. EchoNet-Measurements (JACC, 2025) — trained on 877,983 sonographer annotations from 155,000+ studies — automates 18 standard B-mode and Doppler parameters with accuracy comparable to expert sonographers (R² 0.97 — 0.99).

EchoPrime12M+ pairs
Measurements18 automated
Validation5 health systems
Learn more about Precision Reporting
Auto-generated Echo Report STUDY 2410-DU7713 · CSMC Left Ventricle EF 58% · Normal systolic function No regional wall motion abnormalities Valves Mitral: trace regurgitation Aortic: trileaflet, no stenosis Chambers RV size and function: normal AI DRAFT
In development

Pipeline: Valve disease

The same research foundation extends to multi-valve screening. Mitral regurgitation detection was published in Circulation (2024), and automated deep learning phenotyping of tricuspid regurgitation — led by Vrudhula et al. — was published in JAMA Cardiology (2025). Aortic valve work is in active development, with clearance pathways to follow.

MitralCirculation 2024
TricuspidJAMA Cardiology 2025
AorticIn development
See the full pipeline
PIPELINE — GANTT VIEW '20 '21 '22 '23 '24 '25 '26 '27 NOW LVEF AMYLOID CIRRHOSIS REPORTING MITRAL TRICUSPID AORTIC CLEARED VALIDATION RESEARCH PLANNED PEER-REVIEWED BREAKTHROUGH FDA CLEARED

Ten years of peer-reviewed research. Not a slide deck.

Our foundation is a decade of academic work at Stanford and Cedars-Sinai — culminating in the first and only prospective, blinded, randomized clinical trial of AI in cardiology. Here's the evidence trail, in the words of the journals that published it.

Cardiologists and computer scientists who wrote the papers.

InVision is founded and led by the people who authored the foundational literature on AI in echocardiography — not by acquirers of someone else's research. That difference shows up in how our models are built, how they're tested, and how they behave at the bedside.

Practicing clinicians building for clinicians

Dr. Ouyang is an attending cardiologist who reads echoes every week — currently at Kaiser Permanente Northern California and previously at Cedars-Sinai. Our models are designed against real workflow, not inferred from one.

YC-backed, enterprise-ready

Backed by Y Combinator and strategic partners including Alexion (AstraZeneca Rare Disease), with live deployments through partners like HeartLab.

Trained on the deepest dataset in echo AI

Precision LVEF is trained on more echocardiographic videos than any other FDA-cleared echo AI model, giving it unmatched generalizability across scanners and populations.

We aspire to prevent misdiagnosis of rare diseases, democratize expert knowledge to more clinicians, and ensure that excellent care is available to every patient — in every clinical setting.
Dr. David Ouyang, MD
Co-founder, InVision Medical Technology

Bring cleared echo AI into your health system.

Schedule a 30-minute briefing with our clinical and commercial teams. We'll walk through deployment, reimbursement, and the evidence base — tailored to your cardiovascular service line.

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