FDA
Breakthrough Device Designation

Next-gen cardiac intelligence.

Combining personalized calibration, wearables, and AI for proactive heart failure care.

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FDA Breakthrough Device Designation GRANTED March 2026 Learn more Contact The Coredio Blog Read our latest blogs to understand more

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Disclaimer: Coredio CPSE™ has received FDA Breakthrough Device Designation. The device is not yet cleared by the FDA for commercial use. Indications for Use are subject to FDA review under the 510(k) process.