The General Aim is to Implement Clinical Assessment of Overload by Voluntary Bite Force Registration to Enable Future Simple But Precise Risk Assessment to Provide Individualized Treatment Plans.

The general aim of this clinical trial is to implement clinical assessment of overload by bite force registration to enable future simple but precise risk assessment to provide individualized treatment plans. The main questions it aims to answer are: * Can we risk-assess patients regarding overload based on bite force measurement before dental implant treatment? * Can we profile patients based on bite force to tailor precise dental implant treatment for individual patients? * Will this profiling lead to improved prognosis by reduced number of technical and/or biological complications? Participants with dental implant prostheses get their bite force measured and followed every year up to 10 years to see complications.