Effect of Probe Material on Peri-implant Probing

Inclusion Criteria: * Adults (≥18 years) * Presence of at least one single-unit bone-level implant rehabilitated with a screw-retained prosthesis directly connected to the implant (no intermediate abutment) * Implant in function for at least 1 year after prosthetic loading * No pathological bone loss on periapical radiograph (distance from the most coronal rough surface of the implant to the bone crest \< 3 mm) * Ability to understand and sign informed consent * Peri-implant health or mucositis, defined according to the 2017 World Workshop criteria: * Health: no clinical signs of inflammation, lack of profuse (line or drop) bleeding on probing, no increase in probing depth compared to previous records, and no progressive bone loss beyond initial remodeling (\<2 mm). In the absence of previous radiographs, radiographic bone level \<3 mm without bleeding and/or suppuration on probing. * Mucositis: presence of bleeding and/or suppuration on probing, no increase in probing depth compared to previous records, and no bone loss beyond initial remodeling (\<2 mm). In the absence of previous radiographs, radiographic bone level \<3 mm with bleeding and/or suppuration on probing. Exclusion Criteria: * Cement-retained restorations or prostheses that cannot be removed * Systemic antibiotic or anti-inflammatory treatment within the previous 3 months * Pregnancy or lactation * Peri-implant treatment within the previous 3 months * Participation in another clinical trial within the last 30 days