IBO Odontit - IBO - Non-Engaging Temporary Abutment Gold Anodised - Multiunit RP Titanium - # HE-48615 ( WORKFLOW )
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Description
Non-Engaging Temporary HE-48615
DESCRIPTION
IBO Non-Engaging Temporary Abutment, reference HE-48615, Non-Engaging Temporary HE-48615. Designed for chairside fabrication of multi-unit provisional restorations and immediate-load full-arch cases — the Non-Engaging interface allows rotational latitude required for passive fit of splinted multi-implant provisionals.
CLINICAL APPLICATION
Used for multi-implant or full-arch provisional restorations. The Non-Engaging interface gives the rotational latitude required for passive fit of splinted prostheses, where the rigid rotational lock of an engaging interface would force misalignment between non-parallel implants.
PLATFORM & COMPATIBILITY
Used with IBO Multiunit Abutment platforms (HE-48xxx series) — confirm pairing via MFG# in the IBO catalogue.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HE-48615 |
|---|---|
| Brand | IBO |
| Product family | Non-Engaging Temporary Abutment |
| Designation | Non-Engaging Temporary HE-48615 |
| Connection style | Non-Engaging (rotational latitude) |
| Material | Titanium alloy core / machinable provisional collar |
| Indication | Multi-implant / full-arch splinted provisionals |
| Compatibility | IBO Multiunit Abutment platforms |
| 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.
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.