IBO manufactures the 1G TiBase (Non-Engaging) abutment for CAD/CAM-driven prosthetic rehabilitations on the IBO Conical Reactive line (Nobel Active-compatible protocol). The TiBase serves as the Titanium foundation that bonds to a CAD/CAM-milled superstructure (ceramic, zirconia, or hybrid material) to complete the prosthetic restoration.

This reference, HEC-35750, mounts on the NP (Narrow Platform) implant connection at the 1G cementing height and is the Non-Engaging variant — selected when the prosthetic plan calls for multi-unit prosthesis (bridge / framework) where the abutments must seat passively without rotational engagement.

The 1G TiBase (Non-Engaging) is integral to the modern CAD/CAM workflow for implant restorations. The clinical/laboratory team scans the implant position (intra-orally or on the master cast), designs the prosthetic superstructure in CAD software using a matching IBO CAD library, and mills the superstructure from the selected material (zirconia, glass-ceramic, hybrid, or PMMA for provisionals).

The TiBase is then bonded to the milled superstructure with a dental adhesive cement, producing the final restoration. The Non-Engaging interface determines whether the TiBase locks the prosthesis to the implant's anti-rotation feature (single-unit case) or remains passively non-rotational (multi-unit framework).

This 1G TiBase (Non-Engaging) sits on the Conical Reactive NP (Narrow Platform) implant connection, informationally compatible with the Nobel Biocare® NOBEL Active® Ø3.5 protocol. IBO supplies independent compatible prosthetic components; final clinical use must be verified against the implant manufacturer's documentation.

Brand names are trademarks of their respective owners. Ibodontit S.L. is an independent manufacturer with no affiliation, sponsorship or endorsement from the listed brands.

IBO abutment components are machined from medical-grade Ti-6Al-4V ELI Titanium, Grade 5, in compliance with ASTM F136 and ISO 5832-3. This alloy is selected for its biocompatibility, mechanical strength and chemical stability in the oral environment.

The component features a polished/machined surface at the gingival emergence for soft-tissue compatibility, and tightly toleranced connection geometry at the implant interface to ensure prosthetic passivity and seal integrity.

All materials and processes are subject to full traceability from raw material to final validation.

The 1G TiBase is designed for the IBO Digital Library ecosystem. Workflow: 1. Scan the implant position using an IBO Scanbody or compatible scanbody. 2. Design the prosthetic superstructure in your CAD software using the IBO CAD library for this TiBase variant. 3. Mill the superstructure from the selected material. 4. Bond the milled superstructure onto the TiBase with dental adhesive cement. 5. Deliver the completed restoration.

IBO components are supplied in the manufacturer's validated condition for clinical use. Follow the package insert and IBO Instructions for Use for handling, storage and torque protocol. Do not modify the component geometry, surface or connection seat in any way; doing so compromises the prosthetic interface and the regulatory clearance.

Single-use device. Single patient, single procedure. Discard unused components per local biohazard regulations.

IBO operates under ISO 13485:2016 quality management for the manufacturing of medical devices, holds the AEMPS Spanish Agency of Medicines and Medical Devices licence, and every IBO component carries the CE marking MDR, assessed by a Notified Body.

Five quality foundations apply to this component: