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Medinotec Inc SEC Filings

MDNC OTC

Welcome to our dedicated page for Medinotec SEC filings (Ticker: MDNC), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.

Our SEC filing database is enhanced with expert analysis from Rhea-AI, providing insights into the potential impact of each filing on Medinotec's stock performance. Each filing includes a concise AI-generated summary, sentiment and impact scores, and end-of-day stock performance data showing the actual market reaction. Navigate easily through different filing types including 10-K annual reports, 10-Q quarterly reports, 8-K current reports, proxy statements (DEF 14A), and Form 4 insider trading disclosures.

Designed for fundamental investors and regulatory compliance professionals, our page simplifies access to critical SEC filings. By combining real-time EDGAR feed updates, Rhea-AI's analytical insights, and historical stock performance data, we provide comprehensive visibility into Medinotec's regulatory disclosures and financial reporting.

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Medinotec, Inc. reported mixed quarterly results driven by its distribution business and product development progress. The company recorded a $12,972 gain for the quarter ended August 31, 2025 compared with a $5,247 loss in the prior-year quarter, and a $2,819 loss for the six months ending August 31, 2025 versus a $9,399 loss a year earlier, showing narrower losses year-to-date. Revenue concentration remains high: 93% of total revenue for the quarter came from a single distributor in South Africa (up from 89%).

Cash and equivalents stood at $2,248,095 at August 31, 2025 (previously $2,769,686 on February 28, 2025), with $1,830,216 held in the U.S. The company has 11,755,548 common shares outstanding. Product milestones include FDA clearance for the OutFlo Aortic Valve Dilatation Balloon Catheter on March 11, 2025 with a planned U.S. launch in the fourth quarter of this financial year; several other catheter 510(k) submissions and CE/MDR processes remain in progress.

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