No insider purchase over the last 90 days. The latest was filed 13 Mar 2025.
This page follows insider dealings at Nexalin Technology, Inc. as filed with SEC (Form 4), a company from the Healthcare & Pharma sector. No insider at Nexalin Technology, Inc. has published a filing in the past twelve months. The most recent one dates from 30 September 2025.
Since 2022, the database holds 17 purchases and no sales by insiders of the company.
Other companies in the same sector with recent insider buying flagged by our signals: Cooper Companies, Inc. and Cytosorbents Corp. These figures are compiled from regulatory filings published by SEC (Form 4). They describe what insiders did and are not a recommendation.
Entry is the close on the day after publication, the first price a reader could act on. Prices in the listing currency. Past moves are not a forecast.
Analysts rate Nexalin Technology, Inc. Buy (bullish), based on 1 analysts. Average price target: US$15.00.
This score ranks the purchase within its own market. A position size is suggested only on the venues of the backtested strategy universe; elsewhere, signals stay on watch. Not investment advice.
FY ended December 2025 · cache
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Nexalin Technology, Inc. (Nasdaq: NXL) is a U.S.-listed medical device company headquartered in Houston, Texas, United States, and traded on the NASDAQ Capital Market. Originally formed as a Nevada corporation in 2010 and later reorganized into a Delaware company in 2021, Nexalin is focused on non-invasive neurostimulation technologies aimed at mental health and neurological conditions. The company’s core proposition is built around proprietary bioelectronic devices and its Deep Intracranial Frequency Stimulation (DIFS™) platform, which it describes as a drug-free approach designed to influence brain activity without relying on psychotherapy as the primary intervention. ([sec.gov](https://www.sec.gov/Archives/edgar/data/0001527352/000182912626002673/nexalintech_10k.htm?utm_source=openai))
From an operating standpoint, Nexalin develops and commercializes neurostimulation products positioned for indications such as anxiety, insomnia, and depression, while increasingly broadening its clinical narrative toward traumatic brain injury, PTSD, Alzheimer’s disease, dementia, ADHD, and substance-use disorders. Its product portfolio and messaging have centered on Gen-1 systems as well as newer-generation solutions including Gen-2 SYNC and HALO™, with an emphasis on patient usability, clinical data capture, remote monitoring, and virtual clinic infrastructure that supports research and treatment workflows. ([sec.gov](https://www.sec.gov/Archives/edgar/data/0001527352/000182912626002673/nexalintech_10k.htm?utm_source=openai))
In competitive terms, Nexalin remains a specialized and relatively early-stage player rather than a scaled commercial medtech platform. Its differentiation rests on intellectual property, peer-reviewed clinical publications, and regulatory engagement with the U.S. FDA. The company seeks to position its DIFS technology as a more evidence-based and deeper-acting alternative to more superficial neurostimulation approaches, and it has highlighted U.S. patent protection in substance-use disorder applications as an important strategic asset. ([nexalin.com](https://nexalin.com/nexalin-highlights-its-expanding-body-of-peer-reviewed-neuroimaging-research-confirming-its-difs-technology-as-the-leader-in-evidenced-based-non-invasive-brain-stimulation/?utm_source=openai))
Geographically, Nexalin’s principal executive offices are in Houston, Texas, while investor relations and transfer-agent support are managed through New York. The company’s communications also point to international activity, including leadership meetings in both the U.S. and China, suggesting that expansion potential is not limited to the domestic market. ([sec.gov](https://www.sec.gov/Archives/edgar/data/0001527352/000182912626002673/nexalintech_10k.htm?utm_source=openai))
Recent developments have been central to the investment case. During 2025 and 2026, Nexalin reported additional positive clinical data in Alzheimer’s disease, published peer-reviewed results across multiple indications, advanced a pivotal trial for HALO™ Clarity, secured USPTO patent coverage for substance-use disorders, and completed phases one through five of its virtual clinic and digital ecosystem. At the same time, the company’s 2025 annual report states that it has incurred significant losses and has substantial doubt about its ability to continue as a going concern, underscoring the importance of capital access and execution risk for investors. ([nexalin.com](https://nexalin.com/nexalin-technology-announces-completion-of-phases-one-through-five-of-its-virtual-clinic-and-digital-ecosystem-for-halo-clinical-research-and-patient-management/?utm_source=openai))
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