Welcome to our dedicated page for bioAffinity Tech SEC filings (Ticker: BIAFW), 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.
bioAffinity Technologies, Inc. filings document a public biotechnology company with common stock and tradeable warrants listed on Nasdaq. Recent reports include Form 8-K disclosures for quarterly financial information, CyPath® Lung clinical case-study announcements, annual meeting voting results, director elections, and amendments to the company’s equity incentive compensation plan.
Registration statements and current reports also describe the company’s emerging growth and smaller reporting company status, securities offerings, capital structure, and governance matters associated with its noninvasive lung-disease diagnostics business. The filing record ties operating disclosures to CyPath® Lung, Precision Pathology Laboratory Services, laboratory-developed test commercialization, and the company’s research platform for lung disease diagnostics.
bioAffinity Technologies, Inc. completed a best efforts public offering of 4,000,000 securities, consisting of 1,040,000 shares of common stock and pre-funded warrants to purchase up to 2,960,000 shares, at $0.80 per share or $0.793 per pre-funded warrant, generating gross proceeds of about $3.2 million before fees.
Each pre-funded warrant is immediately exercisable for one share at an exercise price of $0.007 and remains exercisable until used, subject to a 4.99% (or 9.99% at the holder’s election) beneficial ownership cap. The company agreed to 30-day restrictions on additional equity issuances and at-the-market offerings, broader limits on variable rate transactions for three months, and 30-day lock-ups for executives and directors. After the offering, 6,283,061 shares of common stock are outstanding, and proceeds are earmarked for working capital and general corporate purposes.
bioAffinity Technologies, Inc. completed a best efforts public offering of 4,000,000 securities, consisting of 1,040,000 shares of common stock and pre-funded warrants to purchase up to 2,960,000 shares, at $0.80 per share or $0.793 per pre-funded warrant, generating gross proceeds of about $3.2 million before fees.
Each pre-funded warrant is immediately exercisable for one share at an exercise price of $0.007 and remains exercisable until used, subject to a 4.99% (or 9.99% at the holder’s election) beneficial ownership cap. The company agreed to 30-day restrictions on additional equity issuances and at-the-market offerings, broader limits on variable rate transactions for three months, and 30-day lock-ups for executives and directors. After the offering, 6,283,061 shares of common stock are outstanding, and proceeds are earmarked for working capital and general corporate purposes.
bioAffinity Technologies filed Amendment No. 1 to its Registration Statement on Form S-1. The amendment is narrowly focused and is being used to add specific deal-related documents as exhibits, rather than to change the overall terms of the planned offering.
The company is filing the form of Placement Agency Agreement with WallachBeth Capital LLC, along with the form of Pre-Funded Warrant and the form of Placement Agent Warrant, as new exhibits. The rest of the S-1 remains unchanged and is incorporated by reference. The amendment also restates standard undertakings on indemnification of directors and officers and includes updated signature pages from the company’s chief executive officer, chief financial officer, and directors.
bioAffinity Technologies filed Amendment No. 1 to its Registration Statement on Form S-1. The amendment is narrowly focused and is being used to add specific deal-related documents as exhibits, rather than to change the overall terms of the planned offering.
The company is filing the form of Placement Agency Agreement with WallachBeth Capital LLC, along with the form of Pre-Funded Warrant and the form of Placement Agent Warrant, as new exhibits. The rest of the S-1 remains unchanged and is incorporated by reference. The amendment also restates standard undertakings on indemnification of directors and officers and includes updated signature pages from the company’s chief executive officer, chief financial officer, and directors.
bioAffinity Technologies filed an update describing an educational webinar on July 21, 2026, focused on lung health screening and early detection for U.S. veterans at increased risk for lung cancer and other respiratory diseases. The session will cover imaging, noninvasive diagnostics and access to screening and follow-up care.
The webinar is hosted by NAVREF and will feature experts from Philips, bioAffinity Technologies and 4DMedical. Speakers will discuss mobile CT screening, CyPath® Lung testing and advanced functional lung imaging as approaches that may help support earlier detection and clinical decision-making in veteran populations.
The filing also highlights CyPath® Lung, a noninvasive sputum-based test for high-risk patients, which in a published clinical trial showed 92% sensitivity, 87% specificity, 88% accuracy and a 99% negative predictive value for detecting lung cancer in patients with small indeterminate nodules.
bioAffinity Technologies filed an update describing an educational webinar on July 21, 2026, focused on lung health screening and early detection for U.S. veterans at increased risk for lung cancer and other respiratory diseases. The session will cover imaging, noninvasive diagnostics and access to screening and follow-up care.
The webinar is hosted by NAVREF and will feature experts from Philips, bioAffinity Technologies and 4DMedical. Speakers will discuss mobile CT screening, CyPath® Lung testing and advanced functional lung imaging as approaches that may help support earlier detection and clinical decision-making in veteran populations.
The filing also highlights CyPath® Lung, a noninvasive sputum-based test for high-risk patients, which in a published clinical trial showed 92% sensitivity, 87% specificity, 88% accuracy and a 99% negative predictive value for detecting lung cancer in patients with small indeterminate nodules.
bioAffinity Technologies, Inc. is conducting a primary offering of 2,631,579 shares of common stock, together with pre-funded and placement agent warrants and the shares issuable upon their exercise. The assumed price is $1.52 per share, implying estimated net proceeds of about $3.4 million for working capital and general corporate purposes.
The company focuses on noninvasive lung diagnostics, led by its CyPath® Lung test, which showed 92% sensitivity, 87% specificity, and 88% accuracy for small pulmonary nodules in a clinical trial. CyPath® Lung unit sales grew 146% year over year in first-quarter 2026, and a new multicenter clinical trial began enrolling in March 2026.
bioAffinity reported $1.4 million in revenue for the quarter ended March 31, 2026, and $6.2 million and $9.4 million in 2025 and 2024, respectively, but had an accumulated deficit of $72.2 million and $3.1 million in cash. Its auditor raised substantial doubt about its ability to continue as a going concern, and management indicates existing cash supports operations only through June 2026 without additional financing.
bioAffinity Technologies, Inc. is conducting a primary offering of 2,631,579 shares of common stock, together with pre-funded and placement agent warrants and the shares issuable upon their exercise. The assumed price is $1.52 per share, implying estimated net proceeds of about $3.4 million for working capital and general corporate purposes.
The company focuses on noninvasive lung diagnostics, led by its CyPath® Lung test, which showed 92% sensitivity, 87% specificity, and 88% accuracy for small pulmonary nodules in a clinical trial. CyPath® Lung unit sales grew 146% year over year in first-quarter 2026, and a new multicenter clinical trial began enrolling in March 2026.
bioAffinity reported $1.4 million in revenue for the quarter ended March 31, 2026, and $6.2 million and $9.4 million in 2025 and 2024, respectively, but had an accumulated deficit of $72.2 million and $3.1 million in cash. Its auditor raised substantial doubt about its ability to continue as a going concern, and management indicates existing cash supports operations only through June 2026 without additional financing.
bioAffinity Technologies, Inc. filed an 8-K to share a press release about an educational webinar hosted by the Society for Advanced Bronchoscopy on CyPath® Lung’s role in detecting and managing early-stage lung cancer. The live event, titled “Navigating Lower Cancer-Risk Nodules in High-Risk Patients with Noninvasive CyPath® Lung Testing,” is scheduled for Tuesday, June 16, at 7 p.m. ET.
The press release explains that CyPath® Lung is a noninvasive sputum test using advanced flow cytometry, a fluorescent porphyrin, and proprietary artificial intelligence to analyze the lung microenvironment. In a published clinical trial of high-risk patients with small indeterminate lung nodules less than 20 millimeters, CyPath® Lung showed 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value in detecting lung cancer. The company notes that the test is marketed as a Laboratory Developed Test under CLIA oversight and is intended to be used alongside other clinical findings rather than as a standalone diagnostic.
bioAffinity Technologies, Inc. filed an 8-K to share a press release about an educational webinar hosted by the Society for Advanced Bronchoscopy on CyPath® Lung’s role in detecting and managing early-stage lung cancer. The live event, titled “Navigating Lower Cancer-Risk Nodules in High-Risk Patients with Noninvasive CyPath® Lung Testing,” is scheduled for Tuesday, June 16, at 7 p.m. ET.
The press release explains that CyPath® Lung is a noninvasive sputum test using advanced flow cytometry, a fluorescent porphyrin, and proprietary artificial intelligence to analyze the lung microenvironment. In a published clinical trial of high-risk patients with small indeterminate lung nodules less than 20 millimeters, CyPath® Lung showed 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value in detecting lung cancer. The company notes that the test is marketed as a Laboratory Developed Test under CLIA oversight and is intended to be used alongside other clinical findings rather than as a standalone diagnostic.
bioAffinity Technologies, Inc. reported that it received a notification of allowance from the Mexican Institute of Industrial Property for a patent covering methods of predicting the likelihood of lung cancer using flow cytometry. The patent will protect use of specific antibodies, the porphyrin TCPP, and flow cytometry to detect cancer cells in sputum for the company’s CyPath® Lung test.
CyPath® Lung is a noninvasive, at-home sputum-based test for high-risk patients that uses advanced flow cytometry and artificial intelligence. In a published clinical trial of high-risk patients with small indeterminate lung nodules, CyPath® Lung showed 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value in detecting lung cancer.
bioAffinity Technologies, Inc. reported that it received a notification of allowance from the Mexican Institute of Industrial Property for a patent covering methods of predicting the likelihood of lung cancer using flow cytometry. The patent will protect use of specific antibodies, the porphyrin TCPP, and flow cytometry to detect cancer cells in sputum for the company’s CyPath® Lung test.
CyPath® Lung is a noninvasive, at-home sputum-based test for high-risk patients that uses advanced flow cytometry and artificial intelligence. In a published clinical trial of high-risk patients with small indeterminate lung nodules, CyPath® Lung showed 92% sensitivity, 87% specificity, 88% accuracy and 99% negative predictive value in detecting lung cancer.
bioAffinity Technologies reported that unit sales of its CyPath® Lung diagnostic test reached a record monthly level in April 2026 and increased nearly 300% compared with April 2025, based on preliminary unaudited data. Management said this growth exceeds internal projections and reflects accelerating physician adoption and broader clinical use for lung cancer risk assessment and pulmonary nodule management.
CyPath® Lung is a noninvasive sputum-based test that uses flow cytometry and artificial intelligence to detect malignancy in high‑risk patients. In a clinical trial of patients with small indeterminate lung nodules less than 20 millimeters, the test demonstrated 92% sensitivity, 87% specificity, 88% accuracy and a 99% negative predictive value, which can help avoid unnecessary invasive procedures when results are negative.
bioAffinity Technologies reported that unit sales of its CyPath® Lung diagnostic test reached a record monthly level in April 2026 and increased nearly 300% compared with April 2025, based on preliminary unaudited data. Management said this growth exceeds internal projections and reflects accelerating physician adoption and broader clinical use for lung cancer risk assessment and pulmonary nodule management.
CyPath® Lung is a noninvasive sputum-based test that uses flow cytometry and artificial intelligence to detect malignancy in high‑risk patients. In a clinical trial of patients with small indeterminate lung nodules less than 20 millimeters, the test demonstrated 92% sensitivity, 87% specificity, 88% accuracy and a 99% negative predictive value, which can help avoid unnecessary invasive procedures when results are negative.
bioAffinity Technologies reported first quarter 2026 results, with revenue of $1.4 million and a net loss of $3.6 million, or $(0.81) per share. Revenue declined mainly because the company discontinued certain unprofitable pathology services in March 2025 to focus on higher-margin offerings.
Within that strategy, CyPath® Lung performance was strong. CyPath Lung testing revenue rose about 114% to $361,000 and unit sales increased 146% year-over-year, supported by a 69% increase in ordering physician offices and clinics. Direct costs fell 32% to $0.9 million as earlier cost actions took hold.
Operating expenses grew to $5.0 million from $4.5 million, driven by higher selling, general and administrative spending to scale commercialization, while clinical development costs increased to support a large longitudinal trial funded in part by the U.S. Department of Defense. Cash and cash equivalents were $3.1 million as of March 31, 2026, down from $6.4 million at year-end 2025.
bioAffinity Technologies reported first quarter 2026 results, with revenue of $1.4 million and a net loss of $3.6 million, or $(0.81) per share. Revenue declined mainly because the company discontinued certain unprofitable pathology services in March 2025 to focus on higher-margin offerings.
Within that strategy, CyPath® Lung performance was strong. CyPath Lung testing revenue rose about 114% to $361,000 and unit sales increased 146% year-over-year, supported by a 69% increase in ordering physician offices and clinics. Direct costs fell 32% to $0.9 million as earlier cost actions took hold.
Operating expenses grew to $5.0 million from $4.5 million, driven by higher selling, general and administrative spending to scale commercialization, while clinical development costs increased to support a large longitudinal trial funded in part by the U.S. Department of Defense. Cash and cash equivalents were $3.1 million as of March 31, 2026, down from $6.4 million at year-end 2025.
bioAffinity Technologies, Inc. has filed a resale registration for up to 497,483 shares of common stock on behalf of existing investors. The shares consist of 365,603 warrant shares and 131,880 shares issuable upon conversion of Series B preferred stock after anti-dilution adjustments. The company will not sell shares in this offering and will receive no proceeds from stockholder resales, other than any cash paid if warrants are exercised. As of December 31, 2025, 4,498,675 common shares were outstanding, rising to 4,996,155 shares if all registered warrant and conversion shares are issued. bioAffinity develops noninvasive lung cancer diagnostics, including its CyPath® Lung test, which showed 92% sensitivity and 87% specificity in a clinical trial and recently posted 146% unit sales growth year over year in the first quarter of 2026.
bioAffinity Technologies, Inc. has filed a resale registration for up to 497,483 shares of common stock on behalf of existing investors. The shares consist of 365,603 warrant shares and 131,880 shares issuable upon conversion of Series B preferred stock after anti-dilution adjustments. The company will not sell shares in this offering and will receive no proceeds from stockholder resales, other than any cash paid if warrants are exercised. As of December 31, 2025, 4,498,675 common shares were outstanding, rising to 4,996,155 shares if all registered warrant and conversion shares are issued. bioAffinity develops noninvasive lung cancer diagnostics, including its CyPath® Lung test, which showed 92% sensitivity and 87% specificity in a clinical trial and recently posted 146% unit sales growth year over year in the first quarter of 2026.
bioAffinity Technologies, Inc. reported results of its 2026 Annual Meeting, where stockholders approved several equity and capital structure proposals. They expanded the 2024 Equity Incentive Compensation Plan to reserve 1,000,000 shares, up from 66,666, increasing capacity for stock-based awards. Holders also approved issuances tied to August 2025 warrants and Series B preferred stock, including anti-dilution adjustments that could add hundreds of thousands of shares upon exercise or conversion. Stockholders authorized potential non-public offerings that may trigger a change of control under Nasdaq rules and approved a discretionary 1‑for‑2 to 1‑for‑250 reverse stock split, which the board may implement or abandon. All six director nominees were elected and the independent auditor was ratified.
bioAffinity Technologies, Inc. reported results of its 2026 Annual Meeting, where stockholders approved several equity and capital structure proposals. They expanded the 2024 Equity Incentive Compensation Plan to reserve 1,000,000 shares, up from 66,666, increasing capacity for stock-based awards. Holders also approved issuances tied to August 2025 warrants and Series B preferred stock, including anti-dilution adjustments that could add hundreds of thousands of shares upon exercise or conversion. Stockholders authorized potential non-public offerings that may trigger a change of control under Nasdaq rules and approved a discretionary 1‑for‑2 to 1‑for‑250 reverse stock split, which the board may implement or abandon. All six director nominees were elected and the independent auditor was ratified.