Healthcare professionals specialising in diabetes management consistently advise patients to use only FDA-authorized glucose monitoring devices for making treatment decisions. Organizations including the American Diabetes Association, Diabetes UK,... and the European Association for the Study of Diabetes have not endorsed non-invasive smartwatch technology for glucose monitoring.
For individuals with diabetes, relying on non-validated devices like the Fitsenso TrackPro could lead to inappropriate treatment decisions with potentially serious health consequences. Medical experts emphasize that the convenience of non-invasive monitoring does not outweigh the risks of inaccurate readings.
Disclaimers and Disclosures
The information presented in this document about the Fitsenso TrackPro is based on publicly available data, user reports, and expert analyses as of 18 August 2025. As with any rapidly evolving technology product, specifications, features, and regulatory status may change over time.
In the context of medical devices, blood glucose monitors fall under Class II medical devices, requiring substantial clinical validation and adherence to specific accuracy standards. The Fitsenso TrackPro circumvents these requirements by marketing itself primarily as a wellness device with glucose "estimation" rather than medical-grade "measurement."
This distinction allows the product to be sold without the rigorous testing required for medical devices, but it also means the device cannot legally claim to provide medically reliable glucose readings. Any marketing that suggests or implies medical accuracy for glucose readings potentially violates regulatory guidelines.
Fitsenso TrackPro should not be used for medical diagnosistreatment decisionsmedication dosingor any other clinical purposes. Individuals with diabetes or other conditions requiring accurate
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