KINVENT BIOMECANIQUE

KINVENT BIOMECANIQUE specializes in portable biomechanical analysis systems focused on force-testing. Their primary product category includes devices like the KForce Deltas XL, which are designed for assessing mechanical properties and functional performance in clinical or research environments. These systems help evaluate biomechanical function through controlled force measurements.

KINVENT BIOMECANIQUE operates from the United States. The company’s headquarters and production facilities are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

Yes, KINVENT BIOMECANIQUE’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for Class I devices, which are the primary classification for their biomechanical analysis systems like the KForce Deltas XL.

KINVENT BIOMECANIQUE’s devices fall under Class I classification, which is the lowest risk category for medical devices. This classification is typically assigned to devices posing minimal potential harm to users, such as portable biomechanical analysis systems like the KForce Deltas XL, which are primarily used for diagnostic or research purposes without invasive procedures.