NeckCare Holding ehf

NeckCare Holding specializes in software and hardware tools for biomechanical function analysis and rehabilitation. Their devices include electronic goniometers and kinesiology sensors, which measure joint movement and muscle function, as well as software platforms like the NeckCare System. These tools are designed to assess and guide neck movement, posture, and rehabilitation exercises, helping users track progress and improve biomechanical function.

NeckCare Holding is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites are not detailed in the available information.

NeckCare Holding’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices authorized for use in the US market, allowing healthcare providers and regulators to identify and verify the devices through their assigned UDI.

NeckCare Holding’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and are subject to general controls, while Class II devices require additional performance standards or special controls due to moderate risk. The classification depends on factors like the device’s intended use, potential risks, and the body area it interacts with.