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

Paid on both sides of the house. Outpatient: CPT Category III code 0932T (effective January 1, 2025) covers adjunctive AI analysis supporting heart failure subtype classification — Precision Cardiac Amyloid is in scope when LVEF is 50% or above, and Precision LVEF establishes that threshold in the same pass. Inpatient: CMS has approved a Medicare New Technology Add-on Payment of up to $2,275 per eligible stay, on top of the MS-DRG, effective October 1, 2026.

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

Standard DICOM in. Any scanner, any PACS.

Vendor-neutral by design: GE, Philips, Siemens, Canon, and handheld POCUS. InVision reads the standard DICOM your lab already produces, so there is no new hardware, no new views, and no acquisition change — it deploys alongside your existing PACS, CVIS, and Epic EHR. Typical implementation is about four weeks from kick-off to go-live.

05

Cloud or on-premise. Your choice, not ours.

InVision runs in your data center or in our validated cloud. PHI never has to leave your network, and on-premise no image data is retained once processing completes. Customer data stays in the United States either way — the deployment model is a procurement and security decision, not a product limitation.

06

Surface the diseases you're missing

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

Rare disease detection · Heart failure · Cardiomyopathy
07

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 Detection 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
ROUTINE ECHO VOLUME AMYLOID FLAGGED ROUTINELY MISSED
Flagship in development Foundation Model Nature 2026 JACC 2025

InVision Precision Reporting

Automated, structured echocardiographic reports built on two complementary open-source foundation models. EchoPrime (Nature, 2026) — 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
Structured Echo Report 18 PARAMS MEASUREMENTS · DRAFT WORDING Left ventricle EF 58% LVIDd 4.8 IVSd 1.0 GLS -19% Normal cavity size and wall thickness with normal systolic function. No regional wall motion abnormality. Right ventricle TAPSE 2.1 S' 12 RVSP 28 Normal RV size and systolic function. No evidence of elevated pulmonary pressures. Mitral valve MR trace E/A 1.2 E/e' 7 Trace mitral regurgitation. Leaflets thin and mobile, no stenosis. Normal diastolic filling pressures. Aortic valve + DOPPLER · IVC AI DRAFT
Breakthrough Device Peer reviewed In development

InVision Precision Cirrhosis

Opportunistic detection 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
In development

InVision Precision VHD

Precision Valvular Heart Disease. The same research foundation extends to multi-valve assessment. 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
Learn more about Precision VHD
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.

We reply within one business day.