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Since 2014, DreaMed has pioneered the first artificial pancreas and became the world's first company to receive FDA clearance for a smart algorithm that provides personalized treatment recommendations. Today, our cutting-edge technology is transforming diabetes management and pushing the boundaries of technology to provide expert-level care for people with diabetes everywhere.

Our Mission

Transforming diabetes management, for everyone – everywhere.

Our inspiration

In 2014, a visionary group of leading endocrinologists, engineers, and data scientists identified a critical gap between medical expertise and real-time patient needs — and seized the opportunity to transform diabetes management for everyone, everywhere.

Our Solution

DreaMed envisions a world where every person with diabetes receives expert-level care, seamlessly and effortlessly. We close the gap between rising patient demand and limited specialist availability by harnessing medical data and delivering personalized treatment - without ever compromising on quality or patient experience. Our goal is to make diabetes management so intuitive and effective that it becomes a subtle, background aspect of daily life - a non-issue.

Our Why

Access to expert medical knowledge in diabetes care remains limited, despite rising demand. Diabetes is a complex and costly condition that requires ongoing, specialized management. However, a significant shortage of endocrinology specialists makes it increasingly difficult for healthcare providers to deliver consistent, high-quality care. This shortage also constrains their ability to scale services or maintain financial sustainability, often resulting in compromised patient outcomes and missed revenue opportunities. There is an urgent need for a scalable approach to deliver specialist-level care without overextending limited clinical resources.

Our Journey

2014
  • DreaMed Diabetes is established
  • Developed the first artificial pancreas
2018

First FDA clearance (DEN170043)

  • Approved for Advisor Pro (now endo.digital), a decision-support tool for Type 1 diabetes patients using CGM and insulin pumps (ages 6-65)
2019

Second FDA clearance (K191370)

  • Removed the upper age limit, allowing Medicare patients to use the system.
2020

Third FDA clearance (K201476)

  • Expanded approval to include glucometers in addition to CGMs for insulin closing decisions.
2021

Fourth FDA clearance (K210561)

  • Approved for both Type 1 and Type 2 diabetes patients, added insulin injection support alongside pumps, and introduced patient mobile app integration.
2022
  • endo.digital released for public use and is adopted by DreaMed's first clients in the U.S. Healthcare System
2024
  • Fifth FDA clearance (K232722)* enables broader insulin treatment support for both Type 1 and Type 2 diabetes patients across multiple therapy types.
  • DreaMed surpasses 5,000 active patients on endo.digital*, marking a significant milestone in real-world adoption.
...

Leadership

DreaMed Leadership Team

Eran Atlas

Eran Atlas

CEO and Co-Founder

We take the way physicians are thinking, turn it into a software that can analyze data and provide a treatment recommendation as if a specialist reviewed the data and made those same recommendations. The intention was we would like to covers many as patients as possible, as many use cases possible, be able to back that up with clinical trials, be able to back it up with FDA clearance. And that's exactly what we did!

Watch Video Meet Our Team

DreaMed Leadership Team

Prof. Moshe

Prof. Moshe Phillip

DreaMed's Chief Science Officer, Co-Founder & Director of Endocrinology at Schneider Chidren's Medical Center.

As the shortage of diabetes experts persists globally, we continue to expand the use cases where we can unleash the power of AI to support patients and providers across all care settings. We are proud of our achievement to use AI to transform patient data into expert level treatment recommendations for yet another use case that meets FDA requirements.

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