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Bodyport

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Bodyport

Predicting and preventing heart disease.

bodyport.com
HQ: San Francisco, CA, USA
11-50
Healthcare

Company research

Public company, workplace, funding, and market signals

Overview

Bodyport is a San Francisco-based digital therapeutics company focused on heart-failure / fluid-management monitoring. Its core product is the FDA-cleared Bodyport Cardiac Scale plus Congestion Index software, which combines hemodynamic biomarkers, a clinical portal, and a patient app to support remote care. Public leadership data are partly stale: older company pages still refer to John Lipman as CEO, while his 2026 LinkedIn profile lists him as a current Bodyport board member after Nov. 2025.

Primary product

Bodyport Cardiac Scale + Congestion Index platform

Founded

2015

Headquarters

120 2nd Street, 2nd Floor, San Francisco, CA 94105, United States

Team size

10-20

Work style

Onsite

Industry

Hospitals and Health Care

Sub-industry

Digital therapeutics / remote cardiac monitoring

Offices

120 2nd Street, 2nd Floor, San Francisco, CA 94105, United States

Business model

B2B medical device + software platform
remote patient monitoring (RPM)
digital therapeutics
clinical SaaS / EHR-integrated care platform

Funding

Stage

Series A

Total raised

$15.8M

Latest round

Series A · Aug 2020

Latest amount

$11.2M

People & investors

Leadership

Corey Centen

Founder, President & CTO

Sarah Smith

Founder & Chief Product Officer

John Lipman

Board Member; former CEO (2022-2025)

Jennifer Young

Chief Revenue Officer

Kivanc Ozonat

Head of Data Science

Daniel Yazdi

Medical Director

Lena Onaka

Head of Customer and Product Operations

Phyllis Whiteley, PhD

Chair, Board of Directors

Investors

Boehringer Ingelheim Venture Fund
Hardware Club
HCVC
Initialized Capital
Kapor Capital
Playground Global
Regah Ventures
Y Combinator

Work & culture

Mission-driven and evidence-led, with an emphasis on clinical rigor, patient-centered design, and partnerships with health systems and researchers.

Work style

Onsite

Compensation

No public salary bands were found. Third-party salary estimates suggest average US pay around $116.9k per year, with an estimated range near $103k-$132k, but this is not an official company policy.

Benefits

401(k) / retirement benefits
medical, dental, and vision insurance
equity
generous PTO
paid parental leave

Product & market

Pricing

Enterprise / B2B commercial model with device + software + RPM billing support; public pricing not disclosed.

Differentiators

  • —Measures fluid status and hemodynamic biomarkers from a simple home scale step, not a wearable or implant
  • —FDA-cleared noninvasive heart-failure monitoring platform
  • —Congestion Index detected 70% of heart-failure events in published studies, ahead of weight-only monitoring
  • —Combines device, clinical portal, patient app, API integrations, and compliance workflows
  • —Aims to reduce false alerts and support earlier intervention

Technology

cellular-connected device
web-based clinical dashboard
patient app
API-based EHR integration
RPM billing support
HIPAA-compliant workflows
SOC 2-certified system
proprietary Congestion Index algorithm
hemodynamic biomarker sensing through the feet

Customers

Geisinger
Brigham and Women’s Hospital
health systems
cardiology / heart-failure programs
pharmaceutical and medtech partners

Competitors

Abbott CardioMEMS
Endotronix Cordella
AliveCor
iRhythm
Eko
Philips
Omron

Scale & contact

Estimated revenue

$1M-$10M

Estimated monthly visits

854

Traffic estimate as of Jul 2026

partnerships@bodyport.com+1 (650) 200-1557

Latest news

Bodyport Announces Appointment of Jim Pursley to Board of Directors

Bodyport · Nov 2024

Bodyport added Jim Pursley to its board as it described a move into commercialization and growth.

Published Clinical Results Show Non-Invasive Monitoring Technology Predicts Heart Failure Events at Twice the Rate of Conventional Care

PR Newswire · Sep 2024

Journal of Cardiac Failure publication reported that Bodyport’s Congestion Index predicted heart failure events at twice the rate of weight-only monitoring, with an average lead time of 14 days and 38% fewer false alerts.

Heart Failure Monitoring Technology Doubles Sensitivity for Predicting Events While Minimizing False Alerts Versus Standard of Care

PR Newswire · Mar 2024

Late-breaking THT 2024 results from SCALE-HF 1 said Bodyport detected twice as many heart-failure events as weight-based monitoring while generating fewer alerts.

Bodyport and Geisinger to Launch Innovative Heart Failure Monitoring Program

PR Newswire · Aug 2023

Bodyport and Geisinger announced a 12-month pilot using the FDA-cleared cardiac scale and Fluid Alerts for about 200 adult heart-failure patients.

Bodyport Receives FDA Clearance for the Bodyport Cardiac Scale™

Bodyport · Aug 2022

Bodyport announced FDA 510(k) clearance for the Cardiac Scale, a noninvasive biomarker platform for heart function and fluid-status monitoring.

Built In jobs pageClinical portalFDA clearance releaseLinkedIn company pageMedium profileOfficial websitePatient dashboardResearch & PressX accountY Combinator jobs page
SourcesOfficial websiteResearch and PressFDA clearance press releaseJohn Lipman CEO appointmentGeisinger partnership releaseSeries A funding release2024 clinical results release2024 SCALE-HF 1 releaseBuilt In company pageThe Org company page

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