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Magnus Medical

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uuid0000oy9

Namestring
Magnus Medical
Legal namestring
Magnus Medical Inc.
Websiteurl
magnusmed.com
Company typeenum
Private
Founded yearint
2020
Descriptiontext

Magnus Medical is a privately held neurotechnology company founded in 2020 and headquartered in Burlingame, California, that developed and commercializes the SAINT Neuromodulation System — an FDA-cleared, accelerated transcranial magnetic stimulation (TMS) protocol for treatment-resistant Major Depressive Disorder (MDD). The core technology combines a personalized functional MRI brain mapping step with a proprietary targeting algorithm and an accelerated theta-burst stimulation protocol originally developed at Stanford's Brain Stimulation Lab, enabling completion of the full treatment course in five days (ten 10-minute sessions per day with 50-minute intervals) versus the 6–9 weeks required by conventional TMS. The company received FDA Breakthrough Device Designation in October 2021 and 510(k) clearance (K220177) in 2022, and commercially launched SAINT in April 2024.

Magnus generates revenue through one-time hardware/system sales and licensing of the SAINT system to certified healthcare providers (Verified SAINT Providers), with downstream procedure revenue realized at the clinic level. Go-to-market is enterprise field sales targeting psychiatrists, TMS clinics, and academic medical centers, supplemented by a "Find a Provider" patient-facing portal and direct-to-patient awareness marketing (testimonials, clinical evidence, blog content). Treatment is indicated for adult MDD patients who have failed prior antidepressant medication; the company is also advancing a $11.6 million Department of Defense-funded pivotal trial across four U.S. research institutions (UMass Chan, Medical University of South Carolina, Dell Medical School at UT Austin, and Icahn School of Medicine at Mount Sinai) to expand into postpartum depression. The company has reportedly treated over 700 patients and cites a 79% remission rate in treatment-resistant depression cohorts.

The company has raised approximately $114 million across three disclosed funding events (a $25 million Series A in October 2021 co-led by JAZZ Venture Partners and Red Tree Venture Capital, plus two follow-on rounds in March and May 2025 totaling roughly $89 million) and operates a leadership team led by co-founder and CEO Brett Wingeier with co-founder Brandon Bentzley as CSO, and recently added commercial and engineering leadership including a Chief Commercial Officer and VPs of Hardware Engineering, Clinical Affairs, and Marketing. Magnus is actively enforcing its patents covering accelerated theta-burst stimulation protocols through cease-and-desist letters against infringing parties.

Short descriptiontext

Magnus Medical develops and commercializes the FDA-cleared SAINT Neuromodulation System, an accelerated TMS protocol that uses personalized fMRI brain mapping to treat treatment-resistant major depressive disorder in five days, sold to certified psychiatric clinics and academic medical centers.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersBurlingame, United States
HQ citystring
Burlingame
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Keyword5 values
neuromodulation therapy, depression treatment device, transcranial magnetic stimulation, medical device manufacturer, brain stimulation technology
Industry2 codes
1Psychiatry & Medication Management Platforms
CodeHLALAEABPrimaryYes
2Digital Rehabilitation & Physical Therapy Therapeutics
CodeHLACANAJPrimaryNo
NAICS code2 codes
  • Offices of Physicians, Mental Health Specialists621112
  • Outpatient Mental Health and Substance Abuse Centers621420
SIC code2 codes
  • Surgical & Medical Instruments & Apparatus3841
  • Services-Health Services8000
Product category
Neuromodulation Medical Devices
No data
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1SAINT Neuromodulation System / Therapy Delivery
TypeOne Time License
Description

Magnus Medical generates revenue through the commercial sale and deployment of its FDA-cleared SAINT Neuromodulation System to healthcare providers and clinics. Providers purchase or license the system and deliver treatments to patients, with commercial operations launching in April 2024.

magnusmedical.com
2Treatment Procedures
TypeHardware Sales
Description

Revenue is generated from clinical treatment delivery at certified provider locations, where patients receive the 5-day SAINT treatment protocol for major depressive disorder.

biospace.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
Pricing details1 tier
1Treatment pricing varies by provider and location
ModelOtherBilling cadencePay-as-you-go
Notes

Quote-based / Not publicly disclosed

magnusmedical.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1SAINT
Description

SAINT (Stanford Accelerated Intelligent Neuromodulation Therapy) is the first and only FDA-cleared neuromodulation therapy for rapid treatment of Major Depressive Disorder in just five days, using precision transcranial magnetic stimulation with personalized fMRI targeting.

magnusmedical.com
Core offering1 text field

Magnus Medical develops and commercializes the SAINT Neuromodulation System, an FDA-cleared transcranial magnetic stimulation (TMS) therapy for adult patients with Major Depressive Disorder who have not responded adequately to prior antidepressants. The system uses personalized fMRI brain mapping and a proprietary accelerated theta-burst stimulation protocol to deliver treatment over five days (ten 10-minute sessions per day), achieving remission far faster than conventional TMS. Revenue is generated by selling or licensing the SAINT system to a network of Verified SAINT Providers (clinics, hospitals, and psychiatry practices) who deliver the therapy to patients.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 79% remission rate in treatment-resistant depression patients within an average of 2.6 days
+4 more records
Product overview1 text field

Magnus Medical offers a single unified medical device product: the SAINT Neuromodulation System. SAINT is an FDA-cleared transcranial magnetic stimulation therapy for Major Depressive Disorder that achieves remission within five days using a personalized treatment approach. The system consists of an fMRI brain scan consultation, proprietary targeting algorithm, and a 5-day accelerated TMS stimulation protocol (ten 10-minute sessions per day with 50-minute breaks). The therapy is specifically indicated for adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.

Product and service1 record
1SAINT Neuromodulation System
CategoryNeuromodulation Medical Devices
Description

The first and only FDA-cleared neuromodulation therapy for Major Depressive Disorder (MDD) that achieves remission in five days. It is an advanced, targeted form of transcranial magnetic stimulation (TMS) using precision fMRI-guided neuromodulation with personalized brain targeting. Indicated for adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. Sold to healthcare providers and clinics who deliver the 5-day accelerated protocol (ten 10-minute sessions per day with 50-minute breaks) to patients.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-01
Description

Mount Sinai is one of four U.S. research institutions conducting the $11.6 million DoD-funded pivotal clinical trial evaluating SAINT for postpartum depression. The trial tests whether SAINT can deliver rapid, safe, and durable symptom relief for women within 12 months postpartum.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-05
Description

UMass Chan Medical School enrolled the first patient in the multicenter DoD-funded pivotal clinical trial for SAINT in postpartum depression. The randomized controlled trial will enroll up to 192 women across four leading research institutions.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-05
Description

UT Austin is one of four U.S. research institutions participating in the DoD-funded clinical trial for SAINT neuromodulation therapy targeting postpartum depression. The trial builds on prior research showing 79% remission rates in treatment-resistant depression patients.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-02-05
Description

Medical University of South Carolina is one of four leading research institutions involved in the pivotal clinical trial evaluating SAINT for postpartum depression, funded by an $11.6 million Department of Defense grant.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2019-01-01
Description

SAINT was developed by psychiatrists and neuroscientists at Stanford's Brain Stimulation Lab, driven by a mission to reimagine psychiatry and transform how brain conditions are treated. Stanford research formed the basis for SAINT's clinical evidence including randomized controlled trials published in the American Journal of Psychiatry.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Neuronetics is the established market leader in TMS for depression with its NeuroStar device, FDA-cleared and widely reimbursed. It is the most directly comparable peer to Magnus Medical—both target treatment-resistant MDD with TMS, but Magnus differentiates via accelerated 5-day protocols and fMRI-guided personalized targeting.

TypeDirect peer
Description

Brainsway develops Deep TMS systems with FDA clearance for major depressive disorder, OCD, and other indications. It competes directly with Magnus Medical in the TMS-for-depression market and has a broader indication footprint, though its protocol is not as accelerated as SAINT's.

TypeDirect peer
Description

Magstim is a long-standing manufacturer of TMS stimulators used in research and clinical practice. It supplies the underlying TMS hardware technology that many TMS protocols—including SAINT—build upon, making it both a potential supplier and a competitor.

TypeEmerging player
Description

Flow Neuroscience offers a home-use, app-connected TMS device for depression treatment in Europe. It overlaps with Magnus Medical on the depression neuromodulation thesis but pursues a direct-to-consumer, at-home model rather than clinic-based accelerated protocols.

TypeEmerging player
Description

Sooma develops portable transcranial direct current stimulation (tDCS) devices for depression and other psychiatric conditions. While using a different modality (tDCS vs. TMS), it targets similar treatment-resistant depression patient populations with a home-use device.

TypeBroad incumbent
Description

Greenbrook TMS operates one of the largest U.S. networks of TMS treatment centers focused on depression. As a clinic operator and major purchaser of TMS technology, it represents both a potential channel partner and indirect competitor for Magnus Medical's provider network expansion.

TypeOthers
Description

Caputron distributes neurostimulation devices including TMS and tDCS systems to clinicians and consumers. It operates as a channel/adapter in the neuromodulation market, providing distribution infrastructure that overlaps with Magnus Medical's go-to-market through providers and clinics.

TypeDirect peer
Description

MagVenture manufactures TMS systems widely used in both clinical depression treatment and neuroscience research. It is a direct hardware competitor to Magnus Medical in the TMS device category, with FDA-cleared systems for MDD.

9Apollo TMS (formerly TMS Solutions)
TypeRegional player
Description

Apollo TMS focuses on operating and franchising TMS treatment centers across specific U.S. regions. It represents an indirect competitor as a clinic operator that may purchase competing TMS devices (NeuroStar, Brainsway) instead of SAINT for its network.

TypeEmerging player
Description

Ybrain develops wearable neurostimulation devices for depression and cognitive disorders, primarily in Asian markets. While operating in different geographies, it pursues the same broader thesis of technology-enabled depression treatment that Magnus Medical targets.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability2 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles6 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors3 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Magnus Medical

Neuromodulation Medical Devicesmagnusmed.com

Magnus Medical develops and commercializes the FDA-cleared SAINT Neuromodulation System, an accelerated TMS protocol that uses personalized fMRI brain mapping to treat treatment-resistant major depressive disorder in five days, sold to certified psychiatric clinics and academic medical centers.

What Magnus Medical does

Magnus Medical is a privately held neurotechnology company founded in 2020 and headquartered in Burlingame, California, that developed and commercializes the SAINT Neuromodulation System — an FDA-cleared, accelerated transcranial magnetic stimulation (TMS) protocol for treatment-resistant Major Depressive Disorder (MDD). The core technology combines a personalized functional MRI brain mapping step with a proprietary targeting algorithm and an accelerated theta-burst stimulation protocol originally developed at Stanford's Brain Stimulation Lab, enabling completion of the full treatment course in five days (ten 10-minute sessions per day with 50-minute intervals) versus the 6–9 weeks required by conventional TMS. The company received FDA Breakthrough Device Designation in October 2021 and 510(k) clearance (K220177) in 2022, and commercially launched SAINT in April 2024.

Magnus generates revenue through one-time hardware/system sales and licensing of the SAINT system to certified healthcare providers (Verified SAINT Providers), with downstream procedure revenue realized at the clinic level. Go-to-market is enterprise field sales targeting psychiatrists, TMS clinics, and academic medical centers, supplemented by a "Find a Provider" patient-facing portal and direct-to-patient awareness marketing (testimonials, clinical evidence, blog content). Treatment is indicated for adult MDD patients who have failed prior antidepressant medication; the company is also advancing a $11.6 million Department of Defense-funded pivotal trial across four U.S. research institutions (UMass Chan, Medical University of South Carolina, Dell Medical School at UT Austin, and Icahn School of Medicine at Mount Sinai) to expand into postpartum depression. The company has reportedly treated over 700 patients and cites a 79% remission rate in treatment-resistant depression cohorts.

The company has raised approximately $114 million across three disclosed funding events (a $25 million Series A in October 2021 co-led by JAZZ Venture Partners and Red Tree Venture Capital, plus two follow-on rounds in March and May 2025 totaling roughly $89 million) and operates a leadership team led by co-founder and CEO Brett Wingeier with co-founder Brandon Bentzley as CSO, and recently added commercial and engineering leadership including a Chief Commercial Officer and VPs of Hardware Engineering, Clinical Affairs, and Marketing. Magnus is actively enforcing its patents covering accelerated theta-burst stimulation protocols through cease-and-desist letters against infringing parties.

Magnus Medical firmographics

Firmographics
Name
Magnus Medical
Legal name
Magnus Medical Inc.
Website
https://magnusmed.com
Company type
Private
Founded year
2020
Operating status
Operating
Headcount range
11–50 employees
Short description
Magnus Medical develops and commercializes the FDA-cleared SAINT Neuromodulation System, an accelerated TMS protocol that uses personalized fMRI brain mapping to treat treatment-resistant major depressive disorder in five days, sold to certified psychiatric clinics and academic medical centers.
Ownership category
akta.pro rank

Magnus Medical industry classification

Industry
Product category
Neuromodulation Medical Devices
NAICS
Offices of Physicians, Mental Health Specialists (621112), Outpatient Mental Health and Substance Abuse Centers (621420)
SIC
Surgical & Medical Instruments & Apparatus (3841), Services-Health Services (8000)
akta.pro primary industry
Psychiatry & Medication Management Platforms (HLALAEAB)
akta.pro secondary industry
Digital Rehabilitation & Physical Therapy Therapeutics (HLACANAJ)

Keywords

  • Neuromodulation therapy
  • Depression treatment device
  • Transcranial magnetic stimulation
  • Medical device manufacturer
  • Brain stimulation technology

Where Magnus Medical is headquartered

Location

Headquarters

HQ city
Burlingame
HQ country
United States
HQ region
North America

Markets served

Magnus Medical business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Marketing or Sales, Others

Revenue model

  1. SAINT Neuromodulation System / Therapy Delivery: Magnus Medical generates revenue through the commercial sale and deployment of its FDA-cleared SAINT Neuromodulation System to healthcare providers and clinics. Providers purchase or license the system and deliver treatments to patients, with commercial operations launching in April 2024.
  2. Treatment Procedures: Revenue is generated from clinical treatment delivery at certified provider locations, where patients receive the 5-day SAINT treatment protocol for major depressive disorder.

Pricing tiers

ModelBillingPrice
OtherPay-as-you-goTreatment pricing varies by provider and location

Go-to-market motion2 records

Distribution channels3 records

Marketing channels5 records

Magnus Medical product offering

Product offering

Core offering

Magnus Medical develops and commercializes the SAINT Neuromodulation System, an FDA-cleared transcranial magnetic stimulation (TMS) therapy for adult patients with Major Depressive Disorder who have not responded adequately to prior antidepressants. The system uses personalized fMRI brain mapping and a proprietary accelerated theta-burst stimulation protocol to deliver treatment over five days (ten 10-minute sessions per day), achieving remission far faster than conventional TMS. Revenue is generated by selling or licensing the SAINT system to a network of Verified SAINT Providers (clinics, hospitals, and psychiatry practices) who deliver the therapy to patients.

Product overview

Magnus Medical offers a single unified medical device product: the SAINT Neuromodulation System. SAINT is an FDA-cleared transcranial magnetic stimulation therapy for Major Depressive Disorder that achieves remission within five days using a personalized treatment approach. The system consists of an fMRI brain scan consultation, proprietary targeting algorithm, and a 5-day accelerated TMS stimulation protocol (ten 10-minute sessions per day with 50-minute breaks). The therapy is specifically indicated for adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.

Differentiator

Problem solved

Functional benefit

Brands

  • SAINT: SAINT (Stanford Accelerated Intelligent Neuromodulation Therapy) is the first and only FDA-cleared neuromodulation therapy for rapid treatment of Major Depressive Disorder in just five days, using precision transcranial magnetic stimulation with personalized fMRI targeting.

Products and services

  • SAINT Neuromodulation System The first and only FDA-cleared neuromodulation therapy for Major Depressive Disorder (MDD) that achieves remission in five days. It is an advanced, targeted form of transcranial magnetic stimulation (TMS) using precision fMRI-guided neuromodulation with personalized brain targeting. Indicated for adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode. Sold to healthcare providers and clinics who deliver the 5-day accelerated protocol (ten 10-minute sessions per day with 50-minute breaks) to patients.

Quantifiable outcome

  • 79% remission rate in treatment-resistant depression patients within an average of 2.6 days
  • +4 more outcomes

Companies that use Magnus Medical

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles2 records

Magnus Medical technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability2 records

Feature4 records

Magnus Medical partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core.

  • Icahn School of Medicine at Mount SinaicoreStrategic or Co-development Partner · 1 April 2026Mount Sinai is one of four U.S. research institutions conducting the $11.6 million DoD-funded pivotal clinical trial evaluating SAINT for postpartum depression. The trial tests whether SAINT can deliver rapid, safe, and durable symptom relief for women within 12 months postpartum.
  • University of Massachusetts Chan Medical SchoolcoreStrategic or Co-development Partner · 5 February 2026UMass Chan Medical School enrolled the first patient in the multicenter DoD-funded pivotal clinical trial for SAINT in postpartum depression. The randomized controlled trial will enroll up to 192 women across four leading research institutions.
  • Dell Medical School at UT AustincoreStrategic or Co-development Partner · 5 February 2026UT Austin is one of four U.S. research institutions participating in the DoD-funded clinical trial for SAINT neuromodulation therapy targeting postpartum depression. The trial builds on prior research showing 79% remission rates in treatment-resistant depression patients.
  • Medical University of South CarolinacoreStrategic or Co-development Partner · 5 February 2026Medical University of South Carolina is one of four leading research institutions involved in the pivotal clinical trial evaluating SAINT for postpartum depression, funded by an $11.6 million Department of Defense grant.
  • Stanford Brain Stimulation LabcoreStrategic or Co-development Partner · 1 January 2019SAINT was developed by psychiatrists and neuroscientists at Stanford's Brain Stimulation Lab, driven by a mission to reimagine psychiatry and transform how brain conditions are treated. Stanford research formed the basis for SAINT's clinical evidence including randomized controlled trials published in the American Journal of Psychiatry.

Scale indicators6 records

Recent moves6 records

Expansion highlights5 records

Magnus Medical competitors and assessment

Company assessment

Direct peers

  • Neuronetics: Neuronetics is the established market leader in TMS for depression with its NeuroStar device, FDA-cleared and widely reimbursed. It is the most directly comparable peer to Magnus Medical—both target treatment-resistant MDD with TMS, but Magnus differentiates via accelerated 5-day protocols and fMRI-guided personalized targeting.
  • Brainsway: Brainsway develops Deep TMS systems with FDA clearance for major depressive disorder, OCD, and other indications. It competes directly with Magnus Medical in the TMS-for-depression market and has a broader indication footprint, though its protocol is not as accelerated as SAINT's.
  • Magstim: Magstim is a long-standing manufacturer of TMS stimulators used in research and clinical practice. It supplies the underlying TMS hardware technology that many TMS protocols—including SAINT—build upon, making it both a potential supplier and a competitor.
  • MagVenture: MagVenture manufactures TMS systems widely used in both clinical depression treatment and neuroscience research. It is a direct hardware competitor to Magnus Medical in the TMS device category, with FDA-cleared systems for MDD.

Emerging players

  • Flow Neuroscience: Flow Neuroscience offers a home-use, app-connected TMS device for depression treatment in Europe. It overlaps with Magnus Medical on the depression neuromodulation thesis but pursues a direct-to-consumer, at-home model rather than clinic-based accelerated protocols.
  • Sooma: Sooma develops portable transcranial direct current stimulation (tDCS) devices for depression and other psychiatric conditions. While using a different modality (tDCS vs. TMS), it targets similar treatment-resistant depression patient populations with a home-use device.
  • Ybrain: Ybrain develops wearable neurostimulation devices for depression and cognitive disorders, primarily in Asian markets. While operating in different geographies, it pursues the same broader thesis of technology-enabled depression treatment that Magnus Medical targets.

Broad incumbents

  • Greenbrook TMS: Greenbrook TMS operates one of the largest U.S. networks of TMS treatment centers focused on depression. As a clinic operator and major purchaser of TMS technology, it represents both a potential channel partner and indirect competitor for Magnus Medical's provider network expansion.

Others

  • Pearson Medical / Caputron: Caputron distributes neurostimulation devices including TMS and tDCS systems to clinicians and consumers. It operates as a channel/adapter in the neuromodulation market, providing distribution infrastructure that overlaps with Magnus Medical's go-to-market through providers and clinics.

Regional players

  • Apollo TMS (formerly TMS Solutions): Apollo TMS focuses on operating and franchising TMS treatment centers across specific U.S. regions. It represents an indirect competitor as a clinic operator that may purchase competing TMS devices (NeuroStar, Brainsway) instead of SAINT for its network.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks7 records

Key highlights7 records

Customer concentration

Magnus Medical compliance and trust

Trust signal

Compliance1 record

Magnus Medical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Magnus Medical leadership team

Management profile

Number of profiles

Profiles6 records

Magnus Medical funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors3 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Magnus Medical M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Magnus Medical

What does Magnus Medical do?

Magnus Medical develops and commercializes the SAINT Neuromodulation System, an FDA-cleared transcranial magnetic stimulation (TMS) therapy for adult patients with Major Depressive Disorder who have not responded adequately to prior antidepressants. The system uses personalized fMRI brain mapping and a proprietary accelerated theta-burst stimulation protocol to deliver treatment over five days (ten 10-minute sessions per day), achieving remission far faster than conventional TMS. Revenue is generated by selling or licensing the SAINT system to a network of Verified SAINT Providers (clinics, hospitals, and psychiatry practices) who deliver the therapy to patients.

Is Magnus Medical a public or private company?

Magnus Medical is a private company. It is classified as venture growth investor backed and is currently operating.

When was Magnus Medical founded?

Magnus Medical was founded in 2020. It employs 11 to 50 people.

Where is Magnus Medical based?

Magnus Medical is headquartered in Burlingame, United States, in the North America region.

How does Magnus Medical make money?

Two revenue lines are on record. SAINT Neuromodulation System / Therapy Delivery is the primary driver. The others are treatment Procedures.

Who are Magnus Medical's main competitors?

Direct peers on record are Neuronetics, Brainsway, Magstim and MagVenture. Emerging players are Flow Neuroscience, Sooma and Ybrain. Greenbrook TMS is listed as a broad incumbent. Pearson Medical / Caputron is listed as an others. Apollo TMS (formerly TMS Solutions) is listed as a regional player.

Does Magnus Medical have an API?

No public API is recorded for Magnus Medical.

What industry is Magnus Medical in?

Magnus Medical's product category is Neuromodulation Medical Devices. Its primary akta.pro industry code is HLALAEAB, Psychiatry & Medication Management Platforms, with a secondary code of HLACANAJ, Digital Rehabilitation & Physical Therapy Therapeutics. Its NAICS code is 621112 and its SIC code is 3841.

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Live signals
Mpo-magMount Sinai Begins Enrollment in Study of Neuromodulation Therapy for Postpartum DepressionThe Icahn School of Medicine at Mount Sinai has begun enrolling patients in a $11.6 million Department of Defense-funded pivotal clinical trial evaluating Magnus Medical's SAINT neuromodulation therapy for postpartum depression. The randomized controlled trial, one of four U.S. sites, will test whether this FDA-cleared brain stimulation treatment—which uses functional MRI to precisely target depression-related brain regions—can provide rapid, safe, and durable symptom relief for women within 12 months postpartum. Unlike many depression studies, the trial does not require participants to have failed existing treatments, potentially enabling earlier intervention for mothers experiencing postpartum depression.Business Wire BlogMagnus Expands Access to 5-Day SAINT® Depression Therapy as Leading Health Systems Scale Nationwide AdoptionMagnus Medical Inc. announced the expansion of its SAINT® Depression Therapy program to leading health systems including Cleveland Clinic, UPMC, and HCA Healthcare, bringing availability to 14 states. The company also reported that expanded payer approvals now provide access for more than 80 million covered lives through Medicare and commercial plans.Mount Sinai Health SystemMount Sinai Enrolling Patients in DoD-Funded Clinical Trial of Drug-Free Neuromodulation Therapy for Postpartum DepressionMount Sinai announced enrollment of its first patient in an $11.6 million Department of Defense-funded pivotal clinical trial evaluating Magnus Medical's SAINT neuromodulation therapy for postpartum depression. The randomized controlled trial, involving four leading research institutions, will test whether this FDA-cleared, non-invasive brain stimulation therapy can deliver rapid, safe, and durable symptom relief for women within 12 months postpartum. The study uses personalized functional MRI targeting and an accelerated 5-day treatment schedule, addressing a gap for faster-acting therapies given that current antidepressants and psychotherapy often act too slowly.Business Wire BlogMagnus Medical Moves to Protect Intellectual Property Behind Breakthrough SAINT Accelerated Depression TherapyMagnus Medical Inc. has sent cease-and-desist letters to companies it alleges are infringing on its patents covering SAINT (Stanford Accelerated Intelligent Neuromodulation Therapy), an FDA-cleared accelerated neuromodulation treatment for major depressive disorder. The company holds exclusive rights to U.S. patents assigned from Stanford University covering accelerated theta-burst stimulation protocols, including U.S. Patent Nos. 10,595,735 and 11,839,455. Magnus Medical stated it will defend its intellectual property against companies commercializing accelerated neuromodulation protocols that infringe upon its patented innovation.UT NewsDepartment of Defense funds UT clinical trial of drug-free postpartum…A Department of Defense-funded $11.6 million clinical trial is underway to test SAINT neuromodulation, a fast-acting, drug-free brain stimulation therapy, for postpartum depression at four U.S. research institutions including the University of Texas at Austin. The trial, led nationally by Magnus Medical, will enroll up to 192 women ages 18-45 and builds on prior research showing 79% remission rates in treatment-resistant depression patients within an average of 2.6 days. Postpartum depression affects approximately 500,000 women annually in the United States, with existing treatments often taking weeks to show benefit and being ineffective for some patients.BioSpaceMagnus Medical Announces First Patient Enrolled at University of Massachusetts in Pivotal DoD-Funded Multisite Study of SAINT for Postpartum DepressionMagnus Medical announced enrollment of the first patient at University of Massachusetts Chan Medical School in a $11.6 million Department of Defense-funded pivotal clinical trial evaluating SAINT neuromodulation therapy for postpartum depression. The randomized controlled trial will enroll up to 192 women across four leading research institutions and will test whether SAINT, already FDA-cleared for major depressive disorder, can provide rapid, safe, and durable symptom relief for women experiencing depression following childbirth without requiring prior antidepressant or psychotherapy treatment failure. The study supports DoD's mission to advance innovative therapies for vulnerable populations including new mothers in military families, with SAINT offering a non-drug intervention that could address the limitations of current PPD treatments affecting approximately 500,000 U.S. women annually.Business Wire BlogMagnus Medical Announces First Patient Enrolled at University of Massachusetts in Pivotal DoD-Funded Multisite Study of SAINT for Postpartum DepressionMagnus Medical announced enrollment of the first patient at University of Massachusetts Chan Medical School in a $11.6 million Department of Defense-funded multi-center pivotal clinical trial evaluating SAINT neuromodulation therapy for postpartum depression. The randomized controlled trial will enroll up to 192 women aged 18-45 at four leading research institutions including MUSC, Dell Med, Mount Sinai, and UMass Chan. SAINT, already FDA-cleared for major depressive disorder, is being tested as a non-drug intervention that could provide rapid symptom relief without the systemic side effects of traditional antidepressants.MorningstarMagnus Medical Announces First Patient Enrolled at University of Massachusetts in Pivotal DoD-Funded Multisite Study of SAINT for Postpartum DepressionMagnus Medical announced enrollment of the first patient at University of Massachusetts Chan Medical School in its $11.6 million DoD-funded pivotal clinical trial evaluating SAINT neuromodulation therapy for postpartum depression. The randomized controlled trial will enroll up to 192 women aged 18–45 across four leading research institutions: UMass Chan, the Medical University of South Carolina, Dell Medical School at UT Austin, and the Icahn School of Medicine at Mount Sinai. SAINT is already FDA-cleared for major depressive disorder, and this trial seeks to establish its safety and efficacy as a rapid, drug-free treatment for mothers suffering depression following childbirth, with enrollment open to women up to 12 months postpartum.CnnA new brain treatment for depression is showing positive resultsA new clinical trial published in World Psychiatry found that SAINT (Stanford Accelerated Intelligent Neuromodulation Therapy), a five-day magnetic brain stimulation treatment for treatment-resistant depression, achieved remission in 50% of 24 participants by one month compared to 21% of the placebo group. The therapy, developed at Stanford University's Brain Stimulation Lab and licensed to Magnus Medical, received FDA clearance in September 2022 and is currently available at 17 clinics across the United States. While the results demonstrate the therapy's potential, experts note that durability varies among patients, insurance coverage remains limited, and costs range from $16,000 to over $30,000 per treatment course.