Glucotrack Announces IDE Submission for U.S. Clinical Study of its Novel Implantable Continuous Blood Glucose Monitoring Technology

Glucotrack submitted an Investigational Device Exemption (IDE) application to the FDA to initiate a U.S. clinical study for its fully implantable continuous blood glucose monitoring (CBGM) technology. The submission marks progress from preclinical development toward clinical evaluation, aiming to provide a long-term, real-time, blood-based monitoring option without an on-body wearable.

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