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    SEC Form SD filed by NeuroOne Medical Technologies Corporation

    12/16/25 5:01:02 PM ET
    $NMTC
    Medical/Dental Instruments
    Health Care
    Get the next $NMTC alert in real time by email
    SD 1 ea0269581-sd_neuroone.htm SPECIALIZED DISCLOSURE REPORT

     

     

    UNITED STATES
    SECURITIES AND EXCHANGE COMMISSION
    Washington, D.C. 20549

     

     

     

    FORM SD
    Specialized Disclosure Report
     

     

     

    NeuroOne Medical Technologies Corporation

    (Exact name of registrant as specified in its charter)

     

     

     

    Delaware   001-40439
    (State or other jurisdiction of incorporation)   (Commission file number)

     

    7599 Anagram
    Dr. Eden Prairie, MN
      55344
    (Address of principal executive offices)   (Zip Code)

     

    Dave Rosa, President and Chief Executive Officer, 952-426-1383

    (Name and telephone number, including area code, of the person to contact in connection with this report)

     

    Check the appropriate box to indicate the rule pursuant to which this form is being filed:

     

    ☒Rule 13p-1 under the Securities Exchange Act (17 CFR 240.13p-1) for the reporting period from January 1 to December 31, 2024.

     

    ¨Rule 13q-1 under the Securities Exchange Act (17 CFR 240.13q-1) for the fiscal year ended _______.

     

     

     

     

     

    Section 1 - Conflict Minerals Disclosure

     

    This Form SD of NeuroOne Medical Technologies Corporation (“we” and “us”) is filed pursuant to Rule 13p-1 promulgated under the Securities Exchange Act of 1934, as amended (the “Rule”), and in accordance with the Instructions to Form SD except, however, that we are relying on the Updated Statement on the Effect of the Court of Appeals Decision on the Conflict Minerals Rule issued by the Division of Corporation Finance of the Securities and Exchange Commission (“SEC”) on April 7, 2017 (the “April 2017 Guidance”). As permitted under the April 2017 Guidance, this Form SD does not address Item 1.01(c) of Form SD.

     

    The Rule was adopted by the SEC under Section 1502 of the Dodd-Frank Wall Street Reform and Consumer Protection Act to implement reporting and disclosure requirements related to “conflict minerals” (defined by the SEC as tantalum, tin, tungsten and gold) (collectively, “3TG Minerals”). Pursuant to the Rule, publicly traded companies must submit a report to the SEC after examining whether 3TG Minerals originating in the Democratic Republic of Congo or adjoining countries (Angola, Burundi, The Central African Republic, The Republic of the Congo, Rwanda, South Sudan, Tanzania, Uganda and Zambia) (together, the “Covered Countries”) are present in the products the company manufactures or contracts to manufacture and if any of such 3TG Minerals are necessary to the functionality or production of such products.

     

    This Form SD covers the period from January 1, 2024 to December 31, 2024 (the “Covered Period”).

     

    Item 1.01 Conflict Minerals Disclosure and Report

     

    Company and Product Overview

     

    We are a medical technology company focused on (i) diagnostic, ablation and deep brain stimulation technology for brain related conditions such as epilepsy and Parkinson’s disease; (ii) ablation and stimulation for pain management throughout the body; and (iii) drug delivery including diagnostic and stimulation capabilities.

     

    In 2024, we distributed three devices to our commercial partner Zimmer Biomet: (i) our Evo cortical electrode technology for recording, monitoring, and stimulating brain tissue for up to 30 days, (ii) our Evo sEEG electrode technology for temporary (less than 30 days) use with recording, monitoring, and stimulation equipment for the recording, monitoring, and stimulation of electrical signals at the subsurface level of the brain, and (iii) our OneRF ablation system for creation of radiofrequency lesions in nervous tissue for functional neurosurgical procedures.

     

    Covered Products

     

    We conducted an analysis of the products that we manufactured or contracted to be manufactured, and found that most of our products fall within the scope of the conflict minerals rules as they contain (or may contain) one or more of the 3TG Minerals. These products include our Evo cortical electrode, our Evo sEEG electrode, and our OneRF ablation system. These products are collectively referred to in this Report as the “Covered Products.”

     

    We and our manufacturing partners relied on third-party suppliers for the provision and development of many of the key components and materials used in the Covered Products, and were several steps removed from the mining and processing of the 3TG Minerals used in the Covered Products. As a result, we relied on our suppliers and manufacturing partners to assist us with our reasonable country of origin inquiry regarding the materials in the components supplied by them and used in the manufacturing of the Covered Products.

     

    Reasonable Country of Origin Inquiry (RCOI)

     

    In accordance with the Rule, we conducted in good faith a RCOI for the Covered Period to determine whether the 3TG Minerals necessary to the functionality or production of our products was sourced from Covered Countries or are from recycled or scrap sources.

     

    We rely on several manufacturers to manufacture our Covered Products (the “Manufacturers”). These Manufacturer relies on suppliers who supply components and materials for multiple products that they manufacture. We do not have direct relationships with any of these suppliers. Given our position in the supply chain as a “downstream” company, the Company has to rely on its Manufacturers to conduct their own survey of their “upstream” supply chain in relation to the conflict minerals used in their products. This inquiry consisted of obtaining a written assurance from the Manufacturers that each of them had performed in good faith its own RCOI. Accordingly, we requested and received from each of the Manufacturers a completed Conflict Minerals Reporting Template (“CMRT”).

     

    1

     

    Determination

     

    Based on responses received, we had reason to believe that 3TG Minerals present in certain of our products may have originated in the Covered Countries and may not be from scrap or recycled sources. We have elected not to file disclosure under Item 1.01(c) of Form SD in accordance with the April 2017 Guidance.

     

    Pursuant to the April 2017 Guidance, we have provided only the disclosure required under the provisions of paragraphs (a) and (b) of Item 1.01 of Form SD.

     

    Additional Information

     

    This Form SD is publicly available at nmtc1.com/investors as well as the SEC’s EDGAR database at www.sec.gov. The content of any website referred to in this Form SD is included for general information only and is not incorporated by reference in this Form SD.

     

    Item 1.02 Exhibit

     

    None.

     

    Section 2 – Resource Extraction Issuer Disclosure

     

    Item 2.01 Resource Extraction Issuer Disclosure and Report

     

    None.

     

    Section 3 – Exhibits

     

    Item 3.01 Exhibits.

     

    None.

     

    2

     

    SIGNATURES

     

    Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the duly authorized undersigned.

     

    Date: December 16, 2025 NEUROONE MEDICAL TECHNOLOGIES CORPORATION
         
      By: /s/ Dave Rosa
        Dave Rosa
        Chief Executive Officer

     

    3

     

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