IBO - Engaging Temporary Abutment height 3mm Gold Anodised - INTHEX NP (3.5mm) NP. Titanium - # HEI-35602
Description
Engaging Temporary HEI-35602
DESCRIPTION
IBO engaging Temporary abutment, reference HEI-35602, Engaging Temporary HEI-35602. Designed for chairside fabrication of provisional restorations and immediate-load cases where rotation is restricted by the engaging connection — used for single-tooth provisionals.
CLINICAL APPLICATION
Used for fabrication of single-implant provisional restorations either immediately at the time of implant placement (immediate provisionalization) or during the integration period. The engaging interface locks rotation, making this abutment specifically suitable for single-tooth provisionals where rotational control of the prosthetic is required for occlusal and aesthetic alignment.
PLATFORM & COMPATIBILITY
Used with IBO Conical Reactive platforms — confirm pairing via MFG# prefix (HEI = Internal Hex / HEC = Conical Reactive Ø3.0/NP/RP/WP / HE = multiunit base).
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HEI-35602 |
|---|---|
| Brand | IBO |
| Product family | Engaging Temporary Abutment |
| Designation | Engaging Temporary HEI-35602 |
| Connection style | Engaging (anti-rotational) |
| Material | Titanium alloy core / machinable provisional collar |
| Indication | Single-implant provisional restorations |
| Compatibility | IBO Conical Reactive / Internal Hex per MFG# prefix |
| 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.
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.