Transforming Critical Care: CytoSorbents’ Blood-Purification Programs Deliver Growing Revenues as DrugSorb-ATR Moves Toward a Mid-2026 FDA Review
Monday, December 15, 2025
11:00 AM – 12:00 PM ET
CytoSorbents has developed blood purification technology for removing toxins and harmful substances from a patient’s blood. The company’s high-margin, plug-and-play disposables integrate cohesively into existing hospital blood pumps, enabling broad clinical use and a durable commercial model.
CytoSorb, used to treat life-threatening conditions in the ICU and during cardiac surgery, delivered third-quarter 2025 revenue of $9.5 million, up 10% year-over-year, with a 70% gross margin. The product is EU-approved with nearly 300,000 devices utilized cumulatively to date across more than 70 countries, supporting expectations for rapid global growth.
The company’s second product, DrugSorb-ATR, is advancing toward a significant regulatory milestone with an expected new De Novo submission in Q1 2026 and an anticipated FDA decision by mid-2026. The submission will incorporate analyses of new real-world data demonstrating effectiveness in clinical practice and reinforces its favorable benefit-to-risk profile. With increased visibility from the FDA, CytoSorbents plans to pursue regulatory approval with Health Canada.
Join Jason Kolbert, Head of Research at D. Boral Capital, Dr. Phillip Chan, CEO of CytoSorbents, and Peter J. Mariani, CFO of CytoSorbents, for a fireside conversation that highlights expanding CytoSorb commercial momentum, the regulatory path for DrugSorb-ATR, the impact of new clinical data on the De Novo submission, and the key financial milestones shaping CytoSorbents’ next phase of continued growth.
Jason Kolbert
Head of Research
D. Boral Capital
Dr. Phillip Chan
CEO
CytoSorbents











