IBO Odontit - Engaging Intraoral Scanbody Zirconia Nitride Coating -Conical Active 3.0 Titanium - # IBO 0301 702

IBO Odontit - Engaging Intraoral Scanbody Zirconia Nitride Coating -Conical Active 3.0 Titanium - # IBO 0301 702
SKU: 483704 - In stock
Quantity:

Minimum quantity is 1.

Manufacturer #
IBO 0301 702
Manufacturer
Model
CONICAL
Package
1pk
In Stock
5

Description

IBO
Connections that Transform

Engaging Intraoral 0301 702

Reference IBO 0301 702 · IBO Intraoral Scanbody · CAD/CAM workflow
Engaging Intraoral 0301 702 — product photo

DESCRIPTION

IBO Intraoral Scanbody for digital impression workflows, reference IBO 0301 702, Engaging Intraoral 0301 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.

Reference: IBO 0301 702 · Engaging Intraoral 0301 702.
Function: digital impression of implant position and rotation via Intraoral 3D scanner.
Geometry: scan-optimized contoured body with reference flat for orientation detection.
Material: biocompatible scan-friendly substrate; reflectance optimized for Intraoral scanner detection.
CAD library: matched IBO Digital Library entry available for prosthetic design software.
Workflow: scan → align in CAD → design abutment / crown / bridge on IBO library → mill or print.

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.

Workflow: 1. Scan with IBO Scanbody → 2. Design with IBO CAD Library → 3. Restore.
Compatible with major Intraoral scanner platforms (consult IBO Digital Libraries page for current support).
Used at the impression visit; removed and stored after the scan.
Re-usable across scan sessions; sterilize between patients per IBO IFU.

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 referenceIBO 0301 702
BrandIBO
Product familyIntraoral Scanbody
DesignationEngaging Intraoral 0301 702
WorkflowDigital Intraoral impression → IBO CAD Library → prosthetic design
MaterialBiocompatible scan-friendly substrate (PEEK or matched material)
CompatibilityIBO Conical Reactive implant platforms + IBO Digital Libraries
Package1pk
RegulatoryCE 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.

ScanIntraoral capture of the Scanbody on the seated implant.
DesignIBO CAD Library entry positions the virtual implant; design proceeds in standard prosthetic CAD.
Restore — mill, print, or fabricate the prosthetic component per the design output.

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.

Material selection — alloys validated for biocompatibility and durability.
Dimensional verification — every batch inspected; functional sampling under fatigue and fracture testing.
Mechanical testing — ISO 14801:2016 fatigue and accelerated-ageing testing under cyclic loads representative of the oral environment.
Biocompatibility validation — cytotoxicity (ISO 10993-5:2009) and intracutaneous testing (ISO 10993-10:2021), following ISO 10993-1:2025 principles.
Service-life guaranteeIBO quality commitment ensures durability and performance across the device's service life.
Product description last updated: May 19, 2026

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