IBO Odontit - - Implant Fixture 5.0D x 13mm Conical REACTIVE RP ( 4.3mm ) WP ( 5.0mm ) (4.3mm) - Roughed & Etched surface - # RA5013
Description
Conical REACTIVE Implant Fixture — Ø5.0 mm × 13mm
DESCRIPTION
ODONTIT manufactures the REACTIVE Implant Fixture line for restorative cases requiring a Conical-connection Implant body at the Wide Platform (WP) class. The Ø5.0 mm Fixture is engineered with a self-tapping apical thread profile and is finished with a roughened and Etched surface intended to support osseointegration. Each Fixture is machined from medical-grade titanium and supplied in the manufacturer's validated condition for clinical use.
This reference, RA5013, delivers a Ø5.0 mm body × 13mm length, with the IBO Conical REACTIVE prosthetic connection in the WP platform.
CLINICAL APPLICATION
The Ø5.0 mm REACTIVE Fixture at the WP (Wide Platform) class is intended for posterior restorative scenarios requiring a wider prosthetic emergence and increased load distribution — including molar sites with adequate bone width, and replacement of single molars where a regular-platform body would under-support the prosthetic emergence. It is also indicated for immediate placement following extraction in molar sites with appropriate primary stability.
Final clinical indication, surgical protocol and prosthetic loading regime must be determined by the treating practitioner based on case-specific bone quality, anatomy and prosthetic plan.
PLATFORM & COMPATIBILITY
The Conical REACTIVE WP connection (Ø5.0 mm) is positioned as informational compatibility with the Nobel Biocare® NOBEL ACTIVE® Ø5.0 system. IBO supplies independent compatible prosthetic components; final clinical use must be verified against the Implant manufacturer's documentation.
| System reference | Platform | IBO REACTIVE equivalent |
|---|---|---|
| Nobel Biocare® NOBEL ACTIVE® (informational) | Ø5.0 | Conical REACTIVE WP (Ø5.0 class) |
| IBO Abutment line | WP | HEC-50xxx series · Multiunit HEC-50300 · Impression coping HEC-50700 |
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 | RA5013 |
|---|---|
| Brand | ODONTIT |
| Product family | Conical REACTIVE Implant Fixture |
| Diameter | Ø5.0 mm |
| Length | 13mm |
| Platform | WP (Wide Platform) |
| Connection type | Conical (REACTIVE) |
| Thread design | Self-tapping |
| surface treatment | Roughened and Etched |
| Body material | Ti-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3) |
| Compatibility (informational) | Nobel Biocare® NOBEL ACTIVE® Ø5.0 |
| Compatible IBO abutment series | HEC-50xxx |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
MATERIALS & surface
IBO exclusively selects Ti-6Al-4V ELI titanium, Grade 5, for medical use, 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.
Raw materials are stored in controlled environments to maintain composition and characteristics throughout the manufacturing chain. The Fixture body is finished with a roughened and Etched surface treatment designed to support bone-to-Implant contact.
All materials and processes comply with current regulations and are subject to full traceability from raw material to final validation.
STERILIZATION & HANDLING
IBO fixtures are 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 Fixture geometry, surface treatment or connection seat in any way; doing so compromises both the prosthetic interface and the regulatory clearance.
Single-use device. Single patient, single procedure. Discard unused fixtures 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 Fixture carries the CE marking MDR, assessed by a Notified Body.
Five quality foundations apply to this Fixture: