About Magnus

We are a neurotechnology company backed by recognized groundbreaking science. We pioneered the first and only FDA-cleared, noninvasive brain stimulation therapy using functional connectivity targeting to bring lasting remission to people living with major depressive disorder (MDD) in just five days.

We’re leading a new era in brain health

Our mission

To restore brain health by making proven, rapid-remission treatment accessible for the millions of people living with depression.

We exist to give people a real way forward. With empathy, precision, and proven results, we’re rewriting the story of brain health treatments—for patients, clinicians, and the entire system around them.

Our vision

To redefine what’s possible in brain health by delivering precise, rapid-acting treatments that eliminate disease and give people back their ability to think, feel, and thrive.

We know that brain health is the starting point and with SAINT® for depression, the route to recovery is finally clear.

Leadership

Our executive team is committed to defining the future of brain health, guided by shared values and a strategic vision to eradicate suffering from brain conditions through groundbreaking science.

Board of Directors

Investors

Our story

Originally developed at Stanford University, SAINT is now licensed exclusively to Magnus Medical to turn a scientific revolution in brain health into real-life impact, offering new hope and healing for millions of people living with brain conditions.

SAINT developed

Psychiatrists and neuroscientists at Stanford’s Brain Stimulation Lab combined targeted therapy with a highly accelerated treatment protocol to stimulate neural networks and rebuild healthy connectivity.

2017

Magnus founded

Stanford licensed SAINT exclusively to Magnus for further development and commercialization of the treatment, expanding access for people in need outside of a clinical research environment.

2020

Landmark clinical trial

Published in the American Journal of Psychiatry, the results of this landmark double-blind randomized controlled trial were groundbreaking and pivotal in achieving FDA clearance for SAINT.

2021

New Technology Add-On Payment

SAINT was granted the first-ever NTAP approval for interventional psychiatry, enabling additional Medicare reimbursement for hospitals.

2023

FDA-clearance

SAINT received 510(k) clearance from the U.S. FDA for the treatment of major depressive disorder (MDD) in adults who have failed to achieve satisfactory improvement from prior antidepressant medications.

2022

Breakthrough designation

The U.S. FDA granted Breakthrough Device Designation to SAINT. This program expedites access to technologies offering more effective treatment for serious conditions.

2021

SAINT commercialization

The official shift of SAINT from a research breakthrough to a commercially available clinical treatment began with early adopters of the technology across the U.S.

2024

New Tech Ambulatory Payment Classification

SAINT was granted NTAPC status for outpatient care, securing a dedicated Medicare payment pathway to support patient access to high-efficacy care.

2024

Series B

This round of funding marked a pivotal step toward scaling SAINT and expanding access to rapid, precision treatment for depression.

2025

Work with purpose

Join our passionate team advancing brain health science with urgency and empathy.