
ODONTIT manufactures the REACTIVE Implant Fixture line for restorative cases requiring a narrow-diameter, Conical-connection Implant body. The Ø3.0 mm Fixture is designed for anterior placements and reduced-ridge applications where a smaller diameter is clinically indicated. Each Fixture is machined from medical-grade titanium and finished with a roughened and Etched surface designed to support osseointegration.
This reference, RA3015, delivers an Ø3.0 mm body × 15mm length, with a self-tapping apical thread geometry and the IBO Conical REACTIVE prosthetic connection.
The Ø3.0 mm REACTIVE Fixture is intended for placements where a reduced-diameter body is clinically appropriate — including lateral incisor sites and lower incisor regions, as well as restorative scenarios involving limited mesio-distal space or reduced bone width. Final clinical indication must be determined by the treating practitioner based on case-specific bone quality, anatomy and prosthetic plan.
The Conical REACTIVE Ø3.0 connection is positioned as informational compatibility with the Nobel Biocare® NOBEL ACTIVE® Ø3.0 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) | Ø3.0 | Conical REACTIVE Ø3.0 (NP-class) |
| IBO Abutment line | Ø3.0 | HEC-30xxx series, HEC-30300 multiunit, HEC-30700 impression coping |
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.
| Manufacturer reference | RA3015 |
|---|---|
| Brand | ODONTIT |
| Product family | Conical REACTIVE Implant Fixture |
| Diameter | Ø3.0 mm |
| Length | 15mm |
| Platform | Ø3.0 (NP-class) |
| 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® Ø3.0 |
| Package | 1pk |
| Regulatory | CE marking MDR · ISO 13485:2016 · AEMPS licence |
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: