The presence of ectopic bone refers to the formation of bony structures in locations where bone tissue is not typically found, including abnormal bone growth around the implant and changes in the shape or contour of surrounding bone structures. This is assessed by the investigator through radiological imaging. Additional information captured if present:

Ectopic bone location: Soft tissue, Ramus, Joint space Shape/contour changes: Present, Absent Unit of Measure: Occurrence rate of ectopic bone.

The inter-incisal opening is the magnitude of the aperture formed between the upper and lower incisors during maximal mouth opening. It is commonly assessed by measuring the distance between the incisal edges of the upper and lower incisors. This metric is relevant in medical and dental evaluations as it estimates the mandibular range of motion and offers diagnostic insights into various orofacial conditions, including temporomandibular joint disorders and restricted jaw mobility.The reference values for MIO can vary among individuals and depend on factors such as age, gender, and overall health. Normal ranges typically fall between 35 to 55 mm. The amount of open bite should be subtracted for the MIO measurement, and in deep bites, the amount of vertical overlap should be added to the measurement for accurate determination of MIO. A larger MIO is considered as better.

The relationship between the device's success rate and the underlying medical condition for up to 10 years could help in understanding how different medical conditions impact the success rate of the TMJ replacement device over time. It could highlight which conditions are associated with better or worse outcomes.

Mean implantation time of the device from surgery until device removal or 10 years, if the device remains in place: Knowing the average duration the device remains in place before removal or up to 10 years can give an indication of the longevity of the device and how well it performs over time.

Surgical operation time evaluates the efficiency of the surgical procedure and will be compared to virtual surgery planning vs. conventional surgeries. Also, it will be useful for potential areas for improvement in the surgical technique.

Total hospital post-operative stay (days) and its association with the underlying medical condition and the device: understanding the length of hospital stay post-surgery and its association with the underlying medical condition and the device can provide insights into recovery times, potential complications, and overall patient outcomes.

Perioperative complications related and unrelated to the TMJ System, including allergic reaction to the anesthetic or titanium (anaphylaxis), complications related to the anesthesia, hematoma, or others.

Intraoperative blood loss is important for patient safety. Monitoring and analyzing this data can help optimize planning and surgical techniques to minimize blood loss and associated risks. Estimated blood loss by visual inspection or gravimetric method.

Technical success of the implantation is defined by the surgeon and indicates whether the TMJ System was implanted according to the pre-operative plan.

This is a binary question if technical success was achieved.

For patients where technical success was not achieved, the following details will be captured:

Nature of Device Problem: Design issues, surgical guide fit, TMJ trial implant, or other (specify).

Surgical response: Adaptation, use of standard devices, or other (specify). Cause identification: Yes/No, with details if Yes.

Consequences: None, life-threatening injury, permanent impairment, prolonged hospitalization, increased intervention time, new surgery, or other (serious or not).

Device Deficiency: Could have led to a serious adverse device effect (SADE)? Yes/No/Unknown.

Unit of Measure: rate of technical success, expressed as the percentage of successful implantations across all patients, with breakdowns for issues that led to a lack of success.

Displacement of the ramus component, evaluated by the investigator, will be assessed using (cone beam) computed tomography scans. The outcome is binary: displacement is either "Yes" or "No." In cases of displacement, additional information such as condylar position relative to the fossa, articular eminence, glenoid fossa, articular disc, or condylar translation or rotation will be captured.

Unit of Measure: Percentage of participants with ramus component displacement.

Postoperative weakness of the temporal branch of the facial nerve is defined as a reduction or loss of motor function affecting the frontalis or orbicularis oculi muscles, observed clinically through facial asymmetry, reduced forehead movement, or brow ptosis. Assessment will be performed according to the site's standard of care practice, for example via standardized facial nerve function grading (e.g., House-Brackmann scale or clinical neurological exam).

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants with clinically confirmed weakness of the temporal branch of the facial nerve (numerator) divided by the total number of study participants (denominator).

Marginal mandibular palsy is defined as partial or complete loss of motor function of the lower lip muscles. Assessment will be performed through clinical examination according to the site's standard of care, e.g. graded using the House-Brackmann scale or similar facial nerve evaluation protocol.

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants with clinically confirmed marginal mandibular branch palsy (numerator) divided by the total number of study participants (denominator).

Total facial palsy refers to complete or near-complete loss of motor function across all branches of the facial nerve on the affected side, typically resulting in inability to raise the eyebrow, close the eye, or move the mouth on that side. Diagnosis will be based on clinical neurological examination according to the site's standard of care, e.g. graded using the House-Brackmann scale or equivalent validated facial nerve grading system.

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants with clinically confirmed total facial nerve palsy (numerator) divided by the total number of study participants (denominator).

Sensory changes refer to altered or diminished sensation in areas innervated by branches of the trigeminal nerve, including the lower lip, tongue, and auriculotemporal region. These may present as numbness, tingling, hypoesthesia, or dysesthesia, and will be assessed through patient-reported symptoms and clinical neurological examination (e.g., light touch and pinprick testing), according to the site's standard of care.

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants with one or more confirmed sensory changes involving the lip, tongue, or auriculotemporal nerve (numerator) divided by the total number of study participants (denominator).

Other general post-operative complications include any adverse events not otherwise categorized,. These events will be recorded and classified according to their nature, severity, and relation to the implant procedure, as assessed by the investigator according to the site's standard of care.

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants experiencing at least one general post-operative complication (numerator) divided by the total number of study participants (denominator).

Stable implant components refer to the retention and proper function of the TMJ implant components, including the plate, screws, and prosthesis, without evidence of loosening, fracture, or migration. The assessment will include clinical examination and radiographic imaging (e.g., X-rays, CT scans), conducted according to the site's standard of care.

Unit of Measure: Percentage of participants (%). The occurrence rate will be calculated as the proportion of participants with stable implant components (no loosening, fracture, or migration) (numerator) divided by the total number of study participants (denominator).

Re-intervention due to implant-related or non-implant-related complications. Unit of Measure: Percentage of participants (%) The re-intervention rate will be calculated as the proportion of participants who undergo re-intervention (numerator) divided by the total number of study participants (denominator).

Angle's classification of malocclusion is a widely recognized system used to categorize dental occlusions based on the relationship between the first molars and the canines. This classification divides malocclusions into three primary categories: Class I, where the first molar relationship is normal but other dental discrepancies may exist; Class II, characterized by a retrognathic relationship of the first molars, often accompanied by overbite; and Class III, where the first molars are positioned more mesially, leading to an underbite. The classification is performed through clinical examination, where the occlusal relationships are assessed, typically using dental casts or intraoral assessments to evaluate the alignment and positioning of the teeth.

Dental status will be recorded as: Edentulous, Complete dentition, or Partial dentition. In the case of partial dentition, missing teeth will be recorded individually using the Fédération Dentaire Internationale (FDI) tooth numbering formula.

Before and after surgery, the evaluation of diet consistency is essential to assess the patient's ability to chew and swallow different types of food, as well as to measure subjective diet limitations. Each participant will undergo a diet consistency evaluation prior to and following surgery. The participants will be asked to indicate which of the following options applies to their diet:

0 = no restrictions at all - normal diet 10 = liquids only

Speech scores will be measured by a Numerical Rating Scale (NRS) ranging from 0 to 5, where 0 represents no function and 5 represents optimal condition. This evaluation will assess the patient's ability to speak comfortably and clearly following the temporomandibular joint implant surgery. The assessment will be conducted at baseline, discharge, and during all follow-up visits to track any improvements or limitations in speech.

The Jaw Function Numerical Rating Scale (NRS) is an 11-point scale used to measure subjective jaw function. The endpoints of the scale represent the extremes of jaw mobility, where 0 indicates normal jaw movement and 10 indicates no jaw movement. This evaluation captures the patient's perception of their functional jaw ability following temporomandibular joint implant surgery and throughout the follow-up period.

The Oral Health Impact Profile-14 (OHIP-14) is a validated 14-item questionnaire used to assess oral health-related quality of life by measuring the frequency of problems across seven domains, including functional limitation, physical pain, psychological discomfort, and social disability. Responses are rated on a Likert-type scale from 0 (never) to 4 (very often), with higher scores indicating greater impact on daily life.

The EuroQoL 5-Dimension 5-Level (EQ-5D-5L) is a standardized questionnaire used to assess health-related quality of life across five dimensions-mobility, self-care, usual activities, pain/discomfort, and anxiety/depression-each with five severity levels. It also includes a visual analog scale (EQ VAS) where patients rate their overall health from "the worst" to "the best health you can imagine." Higher values on the EQ VAS and lower dimension scores indicate better perceived health status.

The Helkimo Clinical Dysfunction Index is a simple and quick test that aids in evaluating key factors such as pain, joint sounds, mandibular mobility, and muscle function to provide a comprehensive understanding of the severity of TMJ dysfunction. It is important to note that while the Helkimo Clinical Dysfunction Index can help assess and evaluate TMJ dysfunction, it is not directly associated with TMJ replacement procedures. From question A to E, 3 options can be chosen with a corresponding value of 0, 1 or 5, where a higher value relates to worse clinical symptoms. These are then summated to categorise the patient in a dysfunction group (range from symptom free to severe dysfunction).

The Patient Satisfaction Numeric Rating Scale (NRS) is a single-item, 11-point scale used to assess the patient's satisfaction with functional and aesthetic outcomes of the surgical procedure. Scores range from 0 (no satisfaction) to 10 (complete satisfaction), with higher scores indicating greater satisfaction.

The Surgeon Satisfaction Numeric Rating Scale (NRS) is a single-item, 11-point scale used to assess the surgeon's satisfaction with the functional and morphological/aesthetic outcomes of the surgical procedure. Scores range from 0 (not satisfied) to 10 (completely satisfied), reflecting the surgeon's evaluation of key aspects such as preoperative planning, intraoperative performance, and postoperative outcomes.

Fracture of the ramus component, evaluated by the investigator, will be assessed using (cone beam) computed tomography scans. The outcome is binary: fracture is either "Yes" or "No." If a fracture is detected, additional descriptive details will captured such as bone discontinuity or interruption, presence of bone fragments or displacement of bone fragments, and changes in alignment or angulation.

Unit of Measure: Percentage of participants with ramus component fracture.

Screw loosening will be evaluated by the investigator using (cone beam) computed tomography scans and reported as a binary outcome (present or not present). For cases where loosening is observed, additional details such as a visible gap between the screw and bone surface, change in screw position, or the presence of radiolucent lines around the screws (indicating potential movement) will be captured.

Unit of Measure: Occurrence rate (%)

Bone resorption or osteolysis of the surrounding bone will be evaluated by the investigator using (cone beam) computed tomography scans. The presence or absence of resorption or osteolysis will be recorded as a binary outcome. If present, additional information will be captured, including thinning of bone around the implant, presence of radiolucent areas indicating bone loss, changes in the shape or contour of bone structures, and any progressive decrease in bone density around the implant components.

Unit of Measure: Occurrence rate (%)

The status of bone grafts (if used) will be evaluated by the investigator through (cone beam) computed tomography scans. The assessment will capture the following:

Integration with native bone: Well Integrated, Partially Integrated, Not Integrated Density of graft material: Normal, Decreased, Increased Volume of graft material: Stable, Decreased, Increased Unit of measurement: rate of occurrence for each of the graft material statuses (e.g., well integrated, partially integrated, not integrated, etc.).