CytoSorbents is commercializing its E.U. approved CytoSorb blood purification technology to treat life-threatening conditions in the intensive care unit and cardiac surgery. The company also seeks U.S. and Canadian approval of a second product, DrugSorb-ATR, to reduce perioperative bleeding risk in patients on blood thinners in cardiac surgery. After FDA denial in April 2025, the company plans to submit a new De Novo application to the FDA in late 2026 or early 2027. Based on $37.1 million in high margin 2025 revenue and the DrugSorb-ATR potential in 2027, we believe CTSO stock to be significantly undervalued at this time.
21 May 2026
CTSO: CytoSorbents reports 1st quarter 2026 results and updates investors on the DrugSorb-ATR De Novo submission to the FDA.
Sign up for free to access
Get access to the latest equity research in real-time from 12 commissioned providers.
Get access to the latest equity research in real-time from 12 commissioned providers.
CTSO: CytoSorbents reports 1st quarter 2026 results and updates investors on the DrugSorb-ATR De Novo submission to the FDA.
- Published:
21 May 2026 -
Author:
Tom Kerr -
Pages:
16 -
CytoSorbents is commercializing its E.U. approved CytoSorb blood purification technology to treat life-threatening conditions in the intensive care unit and cardiac surgery. The company also seeks U.S. and Canadian approval of a second product, DrugSorb-ATR, to reduce perioperative bleeding risk in patients on blood thinners in cardiac surgery. After FDA denial in April 2025, the company plans to submit a new De Novo application to the FDA in late 2026 or early 2027. Based on $37.1 million in high margin 2025 revenue and the DrugSorb-ATR potential in 2027, we believe CTSO stock to be significantly undervalued at this time.