IBO Odontit - Non-Engaging 3G Tibase gingiva height 3mm different cementing height Gold -Conical Active RP ( 4.3mm ) WP ( 5.0mm ) Titanium - # HEC-43744
Description
3G Tibase Abutment — Non-Engaging — Conical Reactive RP & WP (HEC-43744)
DESCRIPTION
IBO manufactures the 3G 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-43744, mounts on the RP & WP (Regular/Wide Platform) implant connection at the 3G 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.
CLINICAL APPLICATION
The 3G 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).
PLATFORM & COMPATIBILITY
This 3G Tibase (Non-Engaging) sits on the Conical Reactive RP & WP (Regular/Wide Platform) implant connection, informationally compatible with the Nobel Biocare® NOBEL Active® Ø4.3 / 5.0 protocol. IBO supplies independent compatible prosthetic components; final clinical use must be verified against the implant manufacturer's documentation.
| Component layer | Reference |
|---|---|
| Host implant body (IBO) | RA43xx and RA50xx (Ø4.3 / Ø5.0 mm Reactive fixtures) |
| This 3G Tibase (Non-Engaging) | HEC-43744 |
| Superstructure | CAD/CAM milled (zirconia / glass-ceramic / hybrid / PMMA provisional) |
| CAD library | IBO RP & WP Tibase 3G library |
| Compatible system (informational) | Nobel Biocare® NOBEL Active® Ø4.3 / 5.0 |
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.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HEC-43744 |
|---|---|
| Brand | IBO |
| Product family | 3G Tibase Abutment |
| Generation | 3G (cementing height variant) |
| Interface | Non-Engaging |
| Connection system | Conical Reactive |
| Platform | RP & WP (Regular/Wide Platform) |
| Application | CAD/CAM superstructure bonding |
| Material | Ti-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3) |
| Finish | Titanium (machined) |
| Host implant series (IBO) | RA43xx and RA50xx (Ø4.3 / Ø5.0 mm Reactive fixtures) |
| Compatibility (informational) | Nobel Biocare® NOBEL Active® Ø4.3 / 5.0 |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
MATERIALS & SURFACE
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.
CAD/CAM INTEGRATION
The 3G 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.
STERILIZATION & HANDLING
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.
QUALITY ASSURANCE
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: