ODONTIT manufactures the REACTIVE Implant Fixture line for restorative cases requiring a Conical-connection Implant body at the Regular Platform (RP) class. The Ø4.3 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, RA4308, delivers a Ø4.3 mm body × 8mm length, with the IBO Conical REACTIVE prosthetic connection in the RP platform.

The Ø4.3 mm REACTIVE Fixture at the RP (Regular Platform) class is the workhorse diameter for restorative scenarios with adequate bone width — including premolar and canine sites, and central incisor positions when ridge anatomy supports a regular-emergence prosthetic profile. It is suited to both single-tooth restorations and as the standard diameter in multi-Implant rehabilitations on the RP platform.

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.

The Conical REACTIVE RP connection (Ø4.3 mm) is positioned as informational compatibility with the Nobel Biocare® NOBEL ACTIVE® Ø4.3 system. IBO supplies independent compatible prosthetic components; final clinical use must be verified against the Implant manufacturer's documentation.

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.

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.

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.

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: