Evaluation of the Safety and Performance of the Neobone®: A Prospective Observational Study in Dental Area

This study aims to collect real-world clinical data to gather information on the performance and safety of the Neobone® when used according to its intended purpose and current clinical applications. The results of the clinical study will serve as clinical evidence for the device's clinical evaluation.

Inclusion Criteria: * Adult males or females (age \> 18 years old); * Patients who are able to sign an informed consent form (for data collection); * Patients undergoing reconstructive dental surgery and indicated for the use of Neobone®; Exclusion Criteria: * Patients who are unable to understand consent and the objectives of the study; * Signs of local or systemic acute/ active or chronic infections; * Metabolic affections; * Severe degenerative diseases, conditions in which general bone grafting is not advisable; * Implementation sites that allow product migration; * Conditions which require structural support in the skeletal system; * Conditions where the implantation site is unstable and not rigidly fixated; * Sensibility to the implantable materials; * Known hypersensitivity to the implant material.