Media Inquiries
Roche Diagnostics U.S. Media Relations
Amy Lynn
1-317-750-7811
Jen Dial
1-463-867-0232
INDIANAPOLIS, March 30, 2026 – Roche announced today the U.S. Food and Drug Administration (FDA) 510(k) clearance of its newest analytical units – the cobas® c 703 and cobas® ISE neo. As part of the scalable and modular cobas® pro integrated solutions, these additions deliver advanced lab-automation capabilities designed to help address some of today’s most pressing laboratory challenges, including staff shortages, limited space and growing test volumes.
These new units reflect Roche’s commitment to leading with science and delivering transformative diagnostic solutions that simplify operations and support faster clinical decision-making. With more than 4,000 cobas® analyzers installed across the U.S., Roche provides laboratories with a standardized platform capable of scaling access to testing quickly and effectively.
The new cobas® c 703 is engineered to double the clinical chemistry throughput1 on cobas® pro integrated solutions, delivering up to 2,000 tests per hour and 70 reagent positions. Its expanded reagent capacity enables more high-value tests to run continuously, reducing reagent reloads and improving workflow efficiency. Monthly operator maintenance further enhances uptime and productivity.
The cobas® ISE neo analytical unit, with up to 1,800 tests per hour, delivers more efficient ISE testing, reducing hands-on time through automated maintenance. The cobas® ISE neo system delivers more tests per reagent bottle, minimizing plastic waste and reducing logistical efforts compared to previous-generation systems. Monthly maintenance supports consistent uptime, helping laboratories manage higher volumes with fewer manual steps.
Together, these units automate tasks traditionally performed manually, supporting laboratories facing staffing shortages while increasing test capacity and accelerating turnaround times.
Launched in the U.S. in 2020, cobas® pro integrated solutions is a modular, scalable system to meet mid- to very-high-volume clinical chemistry and immunochemistry testing needs. The platform drives efficiency through intelligent sample routing, fast STAT assay incubation times, the broadest test menu on an integrated platform, and industry-leading reagent onboard stability.2
Key features include:
With cobas® pro integrated solutions, the required sample volume per test has been reduced by 43% on average compared to previous-generation systems.3 Additionally, the plastic generated per test result has been reduced by up to 78% due to smaller reagent pack sizes and a higher number of tests per pack.4
Founded in 1896 in Basel, Switzerland, as one of the first industrial manufacturers of branded medicines, Roche has grown into the world’s largest biotechnology company and the global leader in in-vitro diagnostics. The company pursues scientific excellence to discover and develop medicines and diagnostics for improving and saving the lives of people around the world. We are a pioneer in personalized healthcare and want to further transform how healthcare is delivered to have an even greater impact. To provide the best care for each person we partner with many stakeholders and combine our strengths in Diagnostics and Pharma with data insights from the clinical practice.
For over 125 years, sustainability has been an integral part of Roche’s business. As a science-driven company, our greatest contribution to society is developing innovative medicines and diagnostics that help people live healthier lives. Roche is committed to the Science Based Targets initiative and the Sustainable Markets Initiative to achieve net zero by 2045.
Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan.
For more information, please visit www.roche.com.
All trademarks used or mentioned in this release are protected by law.
References
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Amy Lynn
1-317-750-7811
Jen Dial
1-463-867-0232
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