Orange Biomed to present home HbA1c testing research at ADA 2026

3 hours ago
Orange Biomed to present home HbA1c testing research at ADA 2026

By AI, Created 5:56 AM UTC, May 27, 2026, /AGP/ – Orange Biomed will present late-breaking research on its microfluidic single-cell technology at the American Diabetes Association’s 86th Scientific Sessions in New Orleans on June 7, 2026. The study focuses on improving reproducibility for home-use HbA1c testing, a key hurdle for more accessible diabetes monitoring.

Why it matters: - Orange Biomed is trying to address one of the biggest barriers to home HbA1c testing: reproducibility. - Better repeatability could make diabetes monitoring more practical outside clinics and broaden access to advanced testing. - The presentation lands on the ADA’s Late-Breaking stage, a slot reserved for urgent, high-impact research.

What happened: - Orange Biomed was selected to present new research at the American Diabetes Association’s 86th Scientific Sessions in New Orleans. - The presentation is scheduled for Sunday, June 7, 2026, at 12:30 PM CT in Poster Hall, Halls D-E. - The study is titled “Improving the Reproducibility of Red Blood Cell Transit Velocity Distributions for HbA1c Estimation Using a Microfluidic Sensor” and is listed as poster #2892-LB. - The company is returning to the ADA Scientific Sessions for the fourth consecutive year.

The details: - Orange Biomed describes itself as a medical technology company behind microfluidic-based single-cell analysis technology. - The company’s flagship platform, OBM rapid A1c, is designed as a microfluidic-based HbA1c testing system for diabetes monitoring. - The research focuses on red blood cell transit velocity distributions as a way to estimate HbA1c. - The ADA Scientific Sessions runs June 5-8, 2026, and is expected to draw more than 12,000 experts from more than 110 countries. - Orange Biomed said the conference is the global stage where the future of diabetes care is shaped. - Orange Biomed is also preparing a 510(k) submission to the FDA for potential over-the-counter clearance, followed by a point-of-care application submission. - The company was recently recognized in Fortune Korea’s “Top 40 Emerging South Korean Healthcare Innovations.” - More information is available on Orange Biomed’s website.

Between the lines: - The ADA late-breaking designation suggests Orange Biomed wants to signal scientific credibility, not just product ambition. - The focus on home-use reproducibility points to a core commercial challenge: consumer testing only scales if results are consistent enough to trust. - The company’s FDA filing plans suggest Orange Biomed is positioning the technology for both consumer and point-of-care markets.

What’s next: - Orange Biomed will present the study on June 7 at the ADA meeting. - The company is expected to continue its U.S. regulatory push with the planned FDA 510(k) submission. - Orange Biomed said it wants to expand access to advanced diabetes care through its single-cell analysis technology.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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