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The BCI Briefing

Company profileNeuromodulation

Motif Neurotech

A miniature, wirelessly powered brain stimulator for treatment-resistant depression.

Location
Houston, United States
Founded
2022
Class
NeuromodulationNot counted among core BCI companies.
Sources last checked
6 Oct 2026

What they are building

Develops DOT, an implant about the size of a blueberry that is seated in the skull above the dura, touches no brain tissue and is powered wirelessly from outside the head.

Signal
ECoG: Local field potentials, including high-gamma activityCortical stim: Electrical pulses through surface contacts
Invasiveness
Minimally invasive
Recording / stimulation
Stimulation
Device
DOT microstimulator — Miniature stimulator seated in the skull above the dura, powered wirelessly
Regulatory status
Investigational; FDA investigational device exemption granted in April 2026
Main use cases
Restore

Where they are clinically

Feasibility

Small early studies that test safety and whether the device can do what it is meant to.

Access today

Clinical study

Accessible only by enrolling in a registered clinical study.

Shown in people
No human result is published. RESONATE, registered for 20 participants, is recruiting.
Still an aim
Stimulation therapy for treatment-resistant depression from an implant seated in the skull.
What stands in the way
Efficacy: a controlled demonstration that stimulation from above the dura relieves depression.

On record here: 1 registered study · 20 participants planned or enrolled · 0 peer-reviewed papers

This technology remains experimental and is not an established treatment. Access is limited to registered clinical studies.

  • 28 Apr 2026US FDA — Investigational device exemption. Permits a clinical study of an investigational device. Not a marketing authorisation.

Why this company matters

Motif shows where therapeutic BCI may scale first: psychiatric indications with very large patient populations and a procedure simpler than a craniotomy. It is a stimulation-first device, a reminder that 'BCI' increasingly covers therapy as well as control. No efficacy result exists yet: RESONATE, with 20 participants planned, is its first clinical trial.

Key milestones

  1. Sep 2026

    RESONATE study registered and recruiting at two US sites; 20 participants planned.

    RESONATE · NCT07594483

  2. 28 Apr 2026

    FDA grants an investigational device exemption for the first clinical trial of DOT, as announced by Rice University.

    Rice University (press release, EurekAlert)

Clinical programmes

  • RESONATE

    Study of a miniature epidural stimulator for depression.

    FeasibilityRecruiting

    20 estimatedNCT07594483

Leadership

  • Jacob Robinson

    Co-founder and CEO

As publicly stated by the organisation. Not a complete list.

IP and patents

3
patent families identified and counted as BCI
2025
earliest first filing among them
3
first filed since 2021; the latest years are incomplete
0 of 3
include a granted member, of those whose family record was read

Across the stack: families by layer

Themes, by number of families: electrodes and arrays (3), stimulation (3), closed loop (2), packaging and hermeticity (1), wireless power (1), wireless telemetry (1). A family can carry several.

Published in: United States (3), counted over the 3 families whose full record was read.

4 kept as adjacent neural technology

Families found for Motif Neurotech in the EPO’s worldwide database, grouped so that one invention counts once. A filing shows what a company sought to protect. It does not show that the technology was built, is in a product, or works in people, and themes are read from titles, abstracts and classes, not from the claims. How to read this

Competitive context

Latest BCI Briefing coverage

Sources

  1. 01

    Brain-computer interface based on Rice research wins FDA approval for first clinical trial (opens in a new tab)

    Company reportedRice University (press release, EurekAlert)28 Apr 2026Checked against source 6 Oct 2026

    A release from the university the company came out of. The approval it reports is an investigational device exemption, which permits a study and is not a marketing authorisation.

  2. 02

    ClinicalTrials.gov NCT07594483 (opens in a new tab)

    Clinical registryClinicalTrials.gov29 Sep 2026Checked against source 3 Oct 2026

    Registry record last updated 2026-09-29.