Nexalin Technology Validates DIFS Technology for Mental Health
Nexalin Technology Inc. saw a significant price increase of 23.24% in pre-market trading as it crossed above its 5-day SMA.
The surge in stock price is attributed to multiple independent peer-reviewed studies confirming the efficacy of Nexalin's Deep Intracranial Frequency Stimulation (DIFS) technology in modulating brain structures related to mood and cognition. This research highlights DIFS's potential to address psychiatric and neurological conditions, providing a non-invasive treatment option that meets the needs of patients seeking alternatives to conventional therapies.
This validation of DIFS technology positions Nexalin as a leader in the non-invasive brain stimulation market, potentially attracting more investors and increasing interest in its innovative treatment solutions.
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- Virtual Clinic Launch: Nexalin, in collaboration with UC San Diego, has launched the NeuroCare® virtual clinic platform aimed at enhancing patient access to treatments for Alzheimer's, mood disorders, and PTSD, which is expected to significantly reduce healthcare costs and improve long-term patient outcomes.
- Device Integration: The integration of the new Gen-3 HALO™ headset with the NeuroCare platform allows patients to receive Deep Intracranial Frequency Stimulation (DIFS™) treatment at home, enhancing privacy and convenience while providing physicians with real-time monitoring tools to optimize patient quality of life.
- Innovative Business Model: The NeuroCare platform operates on a subscription-based model, aiming to transition Nexalin from device sales to long-term patient retention and data-driven revenue growth, marking a significant strategic shift for the company.
- Market Expansion Potential: Nexalin plans to leverage the initial deployment alongside UC San Diego's clinical infrastructure to drive global expansion of its digital health ecosystem, which is expected to lay the foundation for sustainable growth in the global market and reinforce its leadership position in mental health.
- Research Validation: Multiple independent peer-reviewed studies confirm that Nexalin's Deep Intracranial Frequency Stimulation (DIFS) technology can modulate deep brain structures associated with mood and cognition, showcasing its leadership in non-invasive brain stimulation.
- Neuroimaging Evidence: Peer-reviewed neuroimaging research indicates measurable changes in brain activity following treatment, further supporting the efficacy of DIFS technology in mental health treatment.
- Clinical Relevance: Research highlights the potential of DIFS to address psychiatric and neurological conditions where conventional therapies may fall short, meeting the needs of millions of patients worldwide seeking more effective treatments.
- Non-Invasive Advantage: Nexalin's DIFS technology offers a safer and more accessible treatment option without the need for surgery, implants, or pharmaceuticals, aligning with modern healthcare's pursuit of innovation and effectiveness.

- Compliance Notification: Nexalin Technology received a Nasdaq notification on January 21, 2026, indicating non-compliance with the $1 minimum bid price requirement, which could negatively impact investor confidence and market performance.
- Compliance Period: The company has been granted a 180-day compliance period until July 20, 2026, to regain compliance, and failure to meet this requirement may lead to more severe market consequences.
- Operational Evaluation: Nexalin is evaluating operational and financial measures to improve its share price performance, indicating the company's commitment to restoring its stock price and potentially adopting various strategies to enhance market confidence.
- No Reverse Split Consideration: The company is currently not considering a reverse stock split, reflecting management's confidence in the existing capital structure while also indicating a cautious approach to market conditions.

- Nasdaq Warning: Nexalin Technology received a notification on January 21, 2026, from Nasdaq regarding non-compliance with the minimum bid price requirement of $1.00 per share, posing a risk to its continued listing on the exchange.
- Compliance Deadline: The company has been granted 180 days until July 20, 2026, to regain compliance; failure to do so may lead to delisting, which could negatively impact investor confidence and market perception.
- Price Monitoring Measures: In response to the declining stock price, Nexalin intends to continuously monitor its bid price and is considering various strategies to improve its financial position, aiming to mitigate short-term adverse effects on its trading price.
- Product Market Outlook: Nexalin's neurostimulation devices have been approved in China, Brazil, Oman, and Israel, and despite facing stock price pressures, the company remains committed to addressing the global mental health crisis through innovative technology, maintaining its competitive edge in the market.

- Successful FDA Meeting: Nexalin's completion of the Q-Submission meeting with the FDA marks a significant advancement in its clinical development plan for the Gen-2 SYNC™ neurostimulation console aimed at treating Alzheimer's disease.
- Exploring New Pathways: The discussion included the potential use of the De Novo classification pathway, reflecting the innovative mechanism of Nexalin's deep frequency-specific neurostimulation technology, laying the groundwork for future regulatory approvals.
- Clinical Trial Design: Nexalin and the FDA reached alignment on foundational elements of trial design, including patient population and statistical analysis plans, ensuring scientific rigor and efficacy for upcoming pilot and pivotal studies.
- Safety and Efficacy: The Gen-2 SYNC console has demonstrated a favorable safety profile in international trials, with studies indicating significant improvements in cognitive performance for Alzheimer's patients, supporting the company's U.S. development strategy.

Exclusive Distribution Agreement: Nexalin Technology has signed an exclusive distribution agreement with Carmi Masha Technologies to market its Gen-2 Console ("SYNC") neurostimulation device in Israel, following regulatory approval for its use in treating mental health disorders.
Focus on Mental Health Treatment: The SYNC device is designed to provide non-invasive, drug-free treatment for conditions such as insomnia, depression, and anxiety, with potential future applications for PTSD, TBI, and dementia.
Partnership Goals: The collaboration aims to leverage Carmi Masha's expertise in introducing medical technologies to enhance access to Nexalin's innovative solutions in Israel, aligning with the growing demand for effective mental health treatments.
Global Expansion Strategy: This agreement is part of Nexalin's broader strategy to expand its presence in international markets, particularly in the Middle East, while continuing to develop advanced neurostimulation products for mental health issues.






