Clinical Research Directory

Inclusion Criteria: 1. Temporary tooth, from a child ≥ 2 years old, requiring dental restorative treatment with Biodentine™ XP, and/or, Permanent (mature or immature) tooth, from a child or an adult, requiring a dental restorative and/or an endodontic treatment with Biodentine™ XP. 2. Adult patient with a signed informed consent form; For the minor, if in age to understand, an assent is required, and at least one parent or legal representative must consent. 3. Only in France: Subject affiliated or benefiting from a social/health insurance system. Exclusion Criteria: 1. Patient with one or more documented contraindication to use Biodentine™ XP (Refer to IFU). 2. Inadequate expected tooth lifetime as estimated by the investigator: * For a Temporary tooth: high probability of tooth loss within 2 years after treatment with Biodentine™ XP. * For a permanent tooth: high probability of tooth loss within 10 years after treatment with Biodentine™ XP. 3. Patient with any systemic disease that may hinder the normal healing process and/or the follow-up. 4. Adult patient under legal protection measures or unable to express his/her consent, and individual deprived of liberty by judicial or administrative decision, as well as individual receiving psychiatric care. 5. Periodontitis (stage 3, 4 or stage 2 grade C). 6. Inability to comply with study procedures. 7. Participation in another interventional clinical investigation that can induce bias in the study results.