Freedom is engineered to transmit real-time interstitial glucose telemetry directly to a user’s mobile device via integrated Bluetooth Low Energy (BLE), completely eliminating the need for any exterior, on-body transmitter.
The clinical challenge of eliminating an on-body transmitter from an implantable biosensor centers on two core constraints: micro-battery chemistry and RF signal attenuation through biological tissue. Historically, external transmitters served double duty—supplying inductive power to the passive subcutaneous sensor while broadcasting Bluetooth signals through open air to a smartphone.
Freedom retains the core optical, fluorescence-based glucose-sensing chemistry and one-year operational lifespan validated in Eversense 365, while integrating miniaturized active electronics directly into the sub-dermal capsule:
The first-in-human trial is an early feasibility study designed to evaluate basic clinical safety, biological tissue tolerance, and device functionality—specifically real-world BLE packet delivery through human dermis and adipose layers.
The human trial follows pre-clinical animal studies completed during the second quarter of 2026, which tested multiple antenna geometries and anatomical implantation depths. Over approximately seven weeks of continuous logging and more than 18,500 communication data points, the selected antenna configuration achieved a 100% communication success rate within target operational ranges.
Dr. Tim Goodnow, PhD, President and Chief Executive Officer of Senseonics, outlined the commercial thesis: “Now being tested in humans for the first time, the Freedom CGM represents our vision to eliminate the requirement for an on-body component, effectively making continuous glucose monitoring invisible. We believe this represents an extremely attractive proposition for millions of people with diabetes and we are proudly leading the race to get there.
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