Pulling SEC filings + quote and writing the call…

Nexalin Technology, Inc.
Next earnings Aug 4, 2026 · consensus $-0.10 EPS, $90.9K rev
Going-concern penny stock: $302K revenue against an $8.2M loss and a $92.9M deficit — a dilution machine, not an investment.
Revenue $302K · FY2025
Nexalin is a pre-commercial neurostimulation shell trading like a lottery ticket. FY2025 revenue was just $302K — up 79% but off a trivial base, and the five-year history ($144K→$1.32M→$111K→$169K→$302K) shows no durable ramp, only noise. That revenue is legacy Gen-1 device licensing and electrode sales; U.S. marketing of new Gen-1 units has been paused since the FDA's December 2019 CES reclassification, so the real business — Gen-2 SYNC (Alzheimer's/dementia) and Gen-3 HALO (insomnia) — is still in Q-Submission and clinical-trial stage with no clearance and no product revenue. Against that $302K top line the company burned an $8.22M net loss (-2,726% net margin) and -$4.96M of operating cash. The 80% gross margin is meaningless at this scale.
The filing itself removes any ambiguity: management discloses 'substantial doubt about its ability to continue as a going concern,' a failure to meet Nasdaq's minimum bid price (the stock is $0.36), and material weaknesses in internal control over financial reporting (segregation of duties and IT access). The stated plan is to fund operations through an at-the-market (ATM) offering 'though there can be no assurance that sufficient capital will be available on acceptable terms, or at all.' That is the whole story: survival depends on selling stock into a $0.36 tape. Share count already rose 54.7% in one year (13.3M→20.6M) on top of the September 2022 IPO and July 2024 / May 2025 follow-ons — existing holders are being diluted continuously just to keep the lights on.
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| Line item | FY21 | FY22 | FY23 | FY24 | FY25 |
|---|---|---|---|---|---|
| Revenue | $144K | $1.32M | $111K | $169K | $302K |
| Gross profit | $123K | $958K | $85.1K | $132K | $240K |
| Operating income | -$6.02M | -$1.83M | -$5.70M | -$7.75M | -$8.39M |
| Net income | -$6.08M | -$1.70M | -$4.65M | -$7.61M | -$8.22M |
| Diluted EPS | — | -$0.30 | -$0.63 | -$0.83 | -$0.50 |
| Net margin | -4218.9% | -128.5% | -4197.6% | -4508.7% | -2725.8% |
10-year statements — income, cash flow, balance sheet & CSV export →
Annual figures from SEC 10-K XBRL filings. Open the filing links below for full statement detail.
Computed from SEC XBRL annual figures + the current quote. EV and ROIC use long-term + current debt where filed; estimates, not investment advice.
Charter amendment (likely reverse split) to regain Nasdaq minimum bid-price compliance
New financing agreement + unregistered share issuance — dilutive capital raise
Q1'26: ongoing losses, going-concern doubt, ATM-funded operations
Entered new material agreement, touted via Reg FD press release
FY25 net loss $8.2M, going-concern doubt; revenue up 79% to $302K
Reg FD press release — corporate/clinical business update
Received Nasdaq listing deficiency notice (minimum bid price)
Other-events disclosure — business/pipeline update
Q3'25: recurring losses funded by stock sales, cash dwindling
Sources: SEC EDGAR (CIK 0001527352, latest 10-Q filed 2026-05-08) · EODHD · Proprietary analysis · as of 7/4/2026, 9:38:36 AM.
AI-generated analysis, produced by our proprietary engine from SEC filing data.
Investment recommendation produced by TENK/calls (tenkcalls.com), Luxembourg. Completed Jul 4, 2026, 5:38 AM ET. Ratings & methodology: definitions · All recommendations to date: track record · Conflicts: disclosures. Not investment advice.
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