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Ceribell Receives FDA 510(k) Clearance for First-of-its-Kind Delirium Monitoring Solution

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CBLL gets FDA consent for one-of-a-kind delirium monitoring solution

CeriBell Inc. CBLL recently announced that the FDA has given 510(k) clearance for its latest delirium monitoring solution, making it the one and only FDA-cleared solution for continuous tracking of ...
Investing

FDA clears Ceribell’s delirium monitoring system for ICU patients

The company’s delirium algorithm was validated through studies involving 225 adults in critical care environments. "Delirium has been under recognized and under treated in critically ill patients for ...
Taiwan News

Ceribell Receives FDA 510(k) Clearance for First-of-its-Kind Delirium Monitoring Solution

Novel technology paves the way for use of the company's industry-leading point-of-care electroencephalography (EEG) system to address long unmet need in delirium monitoring SUNNYVALE, Calif., Dec. 09, ...
The Globe and Mail

Ceribell Receives FDA 510(k) Clearance for First-of-its-Kind Delirium Monitoring Solution

SUNNYVALE, Calif., Dec. 09, 2025 (GLOBE NEWSWIRE) -- CeriBell, Inc. (Nasdaq: CBLL) (“Ceribell”), a medical technology company focused on transforming the diagnosis and management of patients with ...