July 30. 2025 — Cardiosense, a medical AI company, recently announced that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for the CardioTag device, a multimodal, wearable sensor that simultaneously captures high-fidelity electrocardiogram (ECG), photoplethysmogram (PPG), and seismocardiogram (SCG) signals, empowering clinicians and patients with a comprehensive noninvasive solution to assess cardiac function across care settings.
