Clinical Research Directory

Inclusion Criteria: * Voluntary written informed consent of the participant or their legal authorized representative has been obtained prior to any screening procedures * At least 18 years of age at the time of signing the Informed Consent Form (ICF) * Indication for horizontal and/or vertical bone augmentation in the maxilla or mandible in preparation for implant placement * Sufficient general health to undergo elective oral surgical procedures, as judgjed by the investigator * Ability and willingness to attend all study visits and comply with the protocol requirements. Exclusion Criteria: * Current smoking or use of other nicotine-containing products (eg, e-cigarettes, chewing tobacco) * Presence of uncontrolled systemic diseases that may compromise healing * Ongoing chemotherapy, radiotherapy, or bisposphonate/anti-resorptive therapy in the head or neck region * History of radiation therapy to the jaws * active or untreated periodontal disease, caries or poor oral hygiene * Poorly fitting restorations on teeth adjacent to the augmentation site * Known allergy or hypersensitivity to any material used in the augmentation procedure. * Pregnant or breastfeeding women, or women planning pregnancy during the study period. * Participation in another interventional clinical study within the last 30 days * Any other condition or circumstance that, in the opinion of the investigator, could compromise participant safety, compliance, or the validity of the study results. * Participation in an interventional study with an investigational medicinal product or device.