bioAffinity Technologies Promotes Veteran Awareness and Access to Its Noninvasive CyPath® Lung Cancer Test Through Distribution Partnership with Veteran-Owned AvMEDICAL
bioAffinity Technologies (Nasdaq: BIAF) debuted its federal distribution collaboration with AvMEDICAL by jointly exhibiting CyPath Lung to VA leaders and healthcare professionals.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Companies debut federal distribution collaboration to VA leadership, administrators and physicians at NAVREF 2026
bioAffinity engages GO2 for Lung Cancer network to broaden outreach to veterans at risk
The companies’ nationwide federal healthcare distribution agreement is intended to expand government and agency access to CyPath Lung, bioAffinity Technologies’ noninvasive test for lung cancer, via AvMEDICAL’s established procurement channels, government contracting expertise and existing customer relationships.
"The 2026 NAVREF conference was the perfect venue to debut our distribution agreement with AvMEDICAL and share our companies' commitment to improving healthcare and quality of life for veterans," said Maria Zannes, President and CEO of bioAffinity Technologies. "We look forward to building on the significant interest in CyPath Lung and the many new connections we made with VA physicians and administrators to actively expand veteran awareness and access across the federal healthcare market."
bioAffinity Technologies is a member of NAVREF's Industry Partner Consortium, a collaborative platform to advance VA research.
Responding to a significant health burden among veterans
Lung cancer weighs heavily on the veteran community. The
Extending outreach through the lung cancer screening community
bioAffinity Technologies also presented CyPath Lung to healthcare leaders attending the GO2 for Lung Cancer Centers of Excellence Lung Cancer Screening and Care Conference this week in
The GO2 for Lung Cancer nonprofit organization partners with the VA to work collaboratively to increase awareness of the importance of lung cancer screening for veterans, increase access to screening through its national network of more than 700 screening centers of excellence and provide VA staff with resources for screening implementation, patient education and research programs.
About AvMEDICAL
AvMEDICAL is a Service-Disabled Veteran-Owned Small Business (SDVOSB) that sources premium medical-surgical and laboratory supplies and equipment from top-tier manufacturers to the government healthcare system. Since 2020, AvMEDICAL has more than doubled its product portfolio to provide enhanced product offerings to its federal government customers. The portfolio covers key categories, including remote cardiac monitoring, ultrasound, advanced bedside monitors, infusion systems, incontinence products for both hospital and home use, and best-in-class laboratory and respiratory testing solutions.
About CyPath Lung
CyPath Lung by bioAffinity Technologies is a noninvasive test designed to improve the early detection of lung cancer in patients at high risk for the disease. CyPath Lung uses advanced flow cytometry and proprietary artificial intelligence (AI) to identify cell populations in patient sputum that indicate malignancy. CyPath Lung incorporates a fluorescent porphyrin that is preferentially taken up by cancer and cancer-related cells. In a published clinical trial of high-risk patients, CyPath Lung demonstrated
About bioAffinity Technologies, Inc.
bioAffinity Technologies, Inc. addresses the need for noninvasive diagnosis of early-stage cancer and other diseases of the lung and broad-spectrum cancer treatments. The Company’s first product, CyPath Lung, is a noninvasive test that has shown high sensitivity, specificity and accuracy for the detection of early-stage lung cancer. CyPath Lung is marketed as a Laboratory Developed Test (LDT) by Precision Pathology Laboratory Services, a subsidiary of bioAffinity Technologies. LDTs are overseen under the Clinical Laboratory Improvement Amendments (CLIA), which are administered by the Centers for Medicare & Medicaid Services. For more information, visit www.bioaffinitytech.com.
Forward-Looking Statements
Certain statements in this press release constitute "forward-looking statements" within the meaning of the federal securities laws. Words such as "may," "might," "will," "should," "believe," "expect," "anticipate," "estimate," "continue," "predict," "forecast," "project," "plan," "intend" or similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. These forward-looking statements are subject to various risks and uncertainties, many of which are difficult to predict, that could cause actual results to differ materially from current expectations and assumptions from those set forth or implied by any forward-looking statements. Forward-looking statements in this press release include, but are not limited to, statements regarding the anticipated benefits of the distribution agreement and collaboration with AvMEDICAL, including expected expansion of government and agency access to and adoption of CyPath Lung, and expectations regarding growth in demand for, or use of, CyPath Lung following the NAVREF and GO2 for Lung Cancer conferences. Important factors that could cause actual results to differ materially from current expectations include, among others, the risk that AvMEDICAL and bioAffinity Technologies are unable to realize the anticipated benefits of their distribution agreement, including delays or failure in securing government contracts or procurement approvals; the Company's ability to maintain and expand adoption of CyPath Lung as a Laboratory Developed Test, including compliance with evolving CLIA; the Company's need for additional capital and ability to obtain financing on acceptable terms, or at all; competition from other diagnostic technologies and companies; and other factors discussed in the Company’s Annual Report on Form 10-K for the year ended December 31, 2025, and its subsequent filings with the SEC, including subsequent periodic reports on Forms 10-Q and 8-K. Such forward-looking statements are based on facts and conditions as they exist at the time such statements are made and predictions as to future facts and conditions. While the Company believes these forward-looking statements are reasonable, readers of this press release are cautioned not to place undue reliance on any forward-looking statements. The information in this release is provided only as of the date of this release, and the Company does not undertake any obligation to update any forward-looking statement relating to matters discussed in this press release, except as may be required by applicable securities laws.
View source version on businesswire.com: https://www.businesswire.com/news/home/20260930178247/en/
bioAffinity Technologies
Julie Anne Overton
Director of Communications
investors@bioaffinitytech.com
Source: bioAffinity Technologies, Inc.