PR Newswire · Nov 2025
CAHF named Darmiyan its preferred provider, giving more than 1,300 member facilities access to BrainSee for early brain-health assessment and dementia prevention.
Public company, workplace, funding, and market signals
Darmiyan is a San Francisco-based neurotechnology and public-health company that uses AI plus brain MRI analysis to screen and monitor brain health, with BrainSee as its flagship FDA-approved prognostic test for estimating progression from amnestic mild cognitive impairment to Alzheimer’s dementia.
Primary product
BrainSee
Founded
2016
Headquarters
San Francisco, California, United States
Team size
11-50
Work style
Onsite
Industry
Public Health
Sub-industry
Neurotechnology / brain health diagnostics
Offices
0 jobs at Darmiyan
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Business model
Stage
Series A
Total raised
$14.7M
Latest round
Venture Round · Oct 2023
Latest amount
$3.5M
Leadership
Founder & CEO
Chief Medical & Technology Officer & Co-founder
Co-founder, Product Consultant
Head of Operations
Head of Analytics and Innovation
Director of Operations and Patient Safety
Manager / Business Consultant
Mission-driven, research-heavy team of neuroscientists, data scientists, clinicians, and patient advocates focused on high accuracy, non-invasiveness, seamless integration, and global accessibility in brain health.
Work style
Onsite
Compensation
Public salary estimates suggest roughly $117.5k average annual pay in the U.S., with typical ranges around $103.5k-$132.7k; official compensation bands were not published.
Benefits
Pricing
Not publicly disclosed; BrainSee is sold through a physician-facing portal and third-party sources suggest per-test style pricing.
Differentiators
Technology
Customers
Competitors
Estimated revenue
~$1.6M ARR (GetLatka) to $10M-$25M annual revenue (LeadIQ/other third-party estimates); public estimates conflict.
Estimated monthly visits
813
PR Newswire · Nov 2025
CAHF named Darmiyan its preferred provider, giving more than 1,300 member facilities access to BrainSee for early brain-health assessment and dementia prevention.
PR Newswire · May 2025
FDA approved a 7-year post-market study intended to further validate BrainSee’s safety and effectiveness in diverse populations.
PR Newswire · Dec 2024
Darmiyan said BrainSee and DarmiSpace would be used in the Medicare GUIDE dementia-care model to support early risk assessment and prevention.
PR Newswire · Jan 2024
Darmiyan announced FDA De Novo approval for BrainSee and described the product as a non-invasive, physician-accessible prognostic software tool.
Reportable / Newsfile · May 2021
FDA granted breakthrough status to BrainSee for non-invasive detection and monitoring of Alzheimer’s disease at the early stage of mild cognitive impairment.