IBO - Engaging Intraoral Scanbody Zirconia Nitride Coating - INTHEX NP (3.5mm) NP. Titanium - # IBO 1501 702
Description
Engaging Intraoral 1501 702
DESCRIPTION
IBO Intraoral SCANBODY for digital impression workflows, reference IBO 1501 702, Engaging Intraoral 1501 702. Used with Intraoral 3D scanners to capture implant position and rotation directly in the operatory, eliminating the conventional impression coping and stone-model step.
CLINICAL APPLICATION
Used in fully digital prosthetic workflows for IBO Conical Reactive implants. The SCANBODY seats on the implant connection like an abutment, the Intraoral scanner records its position, and the matching IBO CAD library entry allows the laboratory to design a final abutment, crown, bridge or custom CAD/CAM component directly from the digital scan — no physical impression, no stone model, no transfer coping required.
PLATFORM & COMPATIBILITY
Used with IBO Conical Reactive implant platforms. The SCANBODY geometry is matched to the platform; the IBO CAD Library entry must match the platform to correctly position the virtual implant in design software.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | IBO 1501 702 |
|---|---|
| Brand | IBO |
| Product family | Intraoral SCANBODY |
| Designation | Engaging Intraoral 1501 702 |
| Workflow | Digital Intraoral impression → IBO CAD Library → prosthetic design |
| Material | Biocompatible scan-friendly substrate (PEEK or matched material) |
| Compatibility | IBO Conical Reactive implant platforms + IBO Digital Libraries |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
MATERIALS & SURFACE
Machined from medical-grade Ti-6Al-4V ELI titanium (Grade 5), ASTM F136 / ISO 5832-3, selected for biocompatibility, mechanical strength and chemical stability in the oral environment.
All materials and processes comply with current regulations and are subject to full traceability from raw material to final validation.
CAD/CAM INTEGRATION
IBO maintains Digital Libraries for major CAD/CAM platforms used in dental laboratory and chairside workflows. After scanning the SCANBODY intraorally, import the CAD library matching the implant platform; the library positions a virtual implant analog at the SCANBODY coordinates, allowing direct design of abutments, crowns, bridges, or hybrid bars in standard prosthetic CAD software.
STERILIZATION & HANDLING
Supplied in the manufacturer's validated condition for clinical use. Follow the package insert and IBO Instructions for Use for handling, storage and any chairside preparation steps. Do not modify the geometry or surface in any way; doing so compromises both clinical fit and 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.