T/CAB 0456-2026 Clinical code of practice for additively manufactured titanium mesh in oral implantology and jaw defect reconstruction
T/CAB 0456-2026 Clinical code of practice for additively manufactured titanium mesh in oral implantology and jaw defect reconstruction
Basic Information
Scope
This document establishes the clinical application of additive manufactured titanium mesh in oral implantation and jawbone defect repair, specifying the requirements for indications and contraindications assessment, information collection, virtual design, acceptance of titanium mesh and auxiliary placement devices, surgical implementation, postoperative management and follow-up, and the removal of titanium mesh. This document is applicable to all levels of medical institutions conducting oral implantation and jawbone defect repair treatments, as well as enterprises and relevant technical personnel involved in the design and production of additive manufactured titanium mesh who use it in clinical practice activities for oral implantation and jawbone defect repair. This standard specifies the technical requirements for the clinical application of additive manufactured titanium mesh in oral implantation and jawbone defect repair, including indications and contraindications assessment, information collection, virtual design, acceptance of titanium mesh and auxiliary placement devices, surgical implementation, postoperative management and follow-up, and the removal of titanium mesh, providing a technical basis for standardized clinical application.