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Inclusive® Titanium Abutment Blanks are designed to be used for the production of custom titanium abutments. All digitally designed abutments are intended to be sent to a Prismatik Dentalcraft-validated milling center for manufacture.
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Inclusive® Titanium Abutment Blanks should only be used for the application described.
The following conditions would contraindicate use of Inclusive Titanium Abutment Blanks:
Hybrid abutments (zirconia abutments with titanium base) are contraindicated by the conditions listed above, and in cases with angle correction or gingival height greater than 6 mm. A patient-specific finished device will consist of both the titanium base and zirconia coping.
Inclusive® Titanium Abutment Blanks are shipped NON-STERILE. Non-sterile items must be cleaned, disinfected, and sterilized prior to clinical use, according to a validated method.
The recommended disinfection process is based on ANSI/AAMI ST79 guidelines, as follows:
The recommended sterilization process is based on the ANSI/AAMI/ISO 17665-1 and ANSI/AAMI ST79 guidelines, as follows:
NOTE: The validated procedures require the use of FDA-cleared sterilization trays, wraps, biological indicators, chemical indicators, and other sterilization accessories labeled for the sterilization cycle recommended. The healthcare facility should monitor the sterilizer for the facility according to an FDA-recognized sterility assurance standard such as ANSI/AAMI ST79.
1Oral disinfectant containing Chlorhexidine is recommended; refer to the disinfectant manufacturer's instructions.
Platform: 4.3 mm
Material Composition: Titanium alloy (Ti6Al4V)