Welcome to our dedicated page for Sensus Healthcare SEC filings (Ticker: SRTS), 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.
Locating FDA milestones, clinical trial updates, and recurring revenue details inside Sensus Healthcare’s dense SEC documents can feel like dissecting a treatment manual. When a single 10-K hides segment margins for SRT device sales and a late-night 8-K moves the stock on new reimbursement codes, missing a line item could cost you clarity—or capital. Stock Titan solves this problem by distilling every Sensus Healthcare filing into plain-English highlights the moment it hits EDGAR.
Our AI-powered summaries cut through medical jargon so you immediately grasp how a fresh 10-Q affects device deployment trends or why an 8-K material event matters to future cash flow. Need real-time Sensus Healthcare Form 4 insider transactions? We alert you as executives buy or sell shares, helping you track Sensus Healthcare insider trading Form 4 transactions before the market reacts. Want the full picture? Access every form in one feed—10-K, 10-Q, 8-K, DEF 14A, and Section 16 filings—each tagged with expert notes, key metrics, and cross-links to historical data.
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Michael Sardano, who serves as a director and as President and General Counsel of Sensus Healthcare, Inc. (SRTS), reported a purchase of 1,000 shares of the company's common stock on 08/13/2025 at a reported price of $3.37 per share. After the transaction, his reported direct beneficial ownership totaled 116,839 shares. The Form 4 lists the transaction code as "P" and shows the change as an acquisition.
Sensus Healthcare reported weakening sales and compressed margins in the quarter and year-to-date. Revenue was $7.3 million in Q2 and $15.7 million for the six months, declines of 20.7% and 21.1% versus prior-year periods driven primarily by fewer units sold to a large U.S. customer. Gross profit fell to $2.9 million in Q2 and $7.3 million YTD, and gross margin narrowed to 39.7% for the quarter (from 58.7%) and 46.5% YTD (from 60.8%).
Higher operating expenses outpaced revenue reductions: G&A, selling and marketing, and R&D all increased, with R&D up 127.8% YTD due to lobbying, added headcount and next-generation product development. The company recorded a net loss of $1.037 million in Q2 and a $3.609 million net loss for the six months, compared with net income in the prior-year periods.
Liquidity remains a stabilizing factor: cash and cash equivalents were $22.2 million and the amended revolving credit facility provides $15.0 million of available borrowing capacity with no outstanding borrowings, and the company was in compliance with credit covenants. Material risks disclosed include significant customer concentration (one U.S. customer represented 56% of Q2 revenue and 78% of receivables) and an ongoing DOJ inquiry for which potential costs cannot be estimated.
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