STARTUP PROFILE

BrainsWay

COUNTRY
Israel
FOUNDED
2003
CATEGORY
Neuromodulation
Developing non-invasive deep transcranial magnetic stimulation systems for the treatment of psychiatric and neurological disorders.
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Neurofounders Insights
$   Funding   -
Public
MODALITY
TMS
FORM FACTOR
Headset/cap
INTERFACE DEPTH
Non-invasive
INDICATION
Psychiatry
TARGET USER
Clinicians
REGULATORY STAGE
FDA cleared (510k)
BrainsWay is the most broadly FDA-cleared deep TMS company, with distinct clearances across MDD, OCD, smoking cessation, and anxiety, plus a recent adolescent expansion, giving it the widest approved indication set of any TMS system on the market. As a publicly traded company with established clinical reimbursement pathways, it is best understood as an incumbent platform in non-invasive psychiatric neuromodulation rather than an emerging startup.
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MOST RECENT COVERAGE
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7
Measuring What Works
4 August – 18 August 2026

Brainsway reported record second-quarter results, with revenue up 35% to $17.1 million and adjusted EBITDA more than doubling to $3.5 million. The company shipped a record 125 Deep TMS systems in the quarter, a 42% increase year over year, and raised its full-year guidance. Brainsway makes a non-invasive deep transcranial magnetic stimulation platform for mental health disorders. The results extend a run of steady commercial growth as the company builds out its provider network and treatment indications.

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6
BCI Goes Commercial
21 July – 4 August 2026

Brainsway made a $3M minority equity investment in Radial Health as part of Radial's Series A. Radial operates a management services organisation supporting a national network of Brain Medicine clinics that deliver non-invasive psychiatric treatments including Deep TMS. For Brainsway, the stake continues a strategy of taking positions in mental health provider networks to expand adoption of its technology. It follows a similar minority investment the company made in Hopemark Health earlier this year.

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3
The Big June Data Dump
9 June – 23 June 2026

Brainsway presented its first 12-month durability data for the SWIFT accelerated Deep TMS protocol at the Clinical TMS Society annual meeting. Drawn from patients who completed the company's FDA pivotal trial, the prospective follow-up reported a remission rate above 80% one year after treatment, alongside a decline in severe functional impairment. SWIFT reduces clinic visits by around 70% compared to the standard protocol.

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