IBO Odontit - - Implant Fixture 3.0D x 11,5mm Conical REACTIVE 3.0 (3.0mm) - Roughed & Etched surface - # RA3011

IBO Odontit -  - Implant Fixture 3.0D x 11,5mm Conical REACTIVE 3.0 (3.0mm) - Roughed & Etched surface - # RA3011
IBO Odontit -  - Implant Fixture 3.0D x 11,5mm Conical REACTIVE 3.0 (3.0mm) - Roughed & Etched surface - # RA3011 IBO Odontit -  - Implant Fixture 3.0D x 11,5mm Conical REACTIVE 3.0 (3.0mm) - Roughed & Etched surface - # RA3011 IBO Odontit -  - Implant Fixture 3.0D x 11,5mm Conical REACTIVE 3.0 (3.0mm) - Roughed & Etched surface - # RA3011
SKU: 483659
Quantity:

Minimum quantity is 1.

Manufacturer #
RA3011
Manufacturer
Model
CONICAL
Features
Implant Fixtures
Package
1pk
ETD
6-7 DAYS

Description

ODONTIT
Connections that Transform

Conical REACTIVE Implant Fixture — Ø3.0 × 11,5mm

Reference RA3011 · ODONTIT REACTIVE line · Conical connection · Self-tapping
Conical Reactive Implant Fixture — Ø3.0 × 11,5mm — product photo

DESCRIPTION

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, RA3011, delivers an Ø3.0 mm body × 11,5mm length, with a self-tapping apical thread geometry and the IBO Conical REACTIVE prosthetic connection.

Body diameter: Ø3.0 mm — narrow-platform indication.
Body length: 11,5mm.
Connection: Conical REACTIVE · platform Ø3.0 (NP-class).
Apical design: self-tapping thread profile for primary stability.
surface treatment: roughened and Etched for osseointegration support.
Body material: medical-grade Ti-6Al-4V ELI titanium (Grade 5), ASTM F136 / ISO 5832-3.
Subfamily: Nobel Active-compatible (compatibility informational; verify with manufacturer documentation).

CLINICAL APPLICATION

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.

Restorative indication: single-tooth or fixed-prosthesis support in narrow-ridge anatomy.
Prosthetic loading: per IBO loading protocol and ISO 14801:2016 testing envelope.
Recommended workflow: integrate with IBO Conical REACTIVE abutment line (HEC-30xxx series) or IBO CAD/CAM abutments designed for Ø3.0 platform.
For two-stage protocols pair with the appropriate IBO healing cap and cover screw.

PLATFORM & COMPATIBILITY

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 referencePlatformIBO REACTIVE equivalent
Nobel Biocare® NOBEL ACTIVE® (informational)Ø3.0Conical REACTIVE Ø3.0 (NP-class)
IBO Abutment lineØ3.0HEC-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.

TECHNICAL SPECIFICATIONS

Manufacturer referenceRA3011
BrandODONTIT
Product familyConical REACTIVE Implant Fixture
DiameterØ3.0 mm
Length11,5mm
PlatformØ3.0 (NP-class)
Connection typeConical (REACTIVE)
Thread designSelf-tapping
surface treatmentRoughened and Etched
Body materialTi-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3)
Compatibility (informational)Nobel Biocare® NOBEL ACTIVE® Ø3.0
Package1pk
RegulatoryCE 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:

Material selection — alloys and surface treatments validated for biocompatibility and durability.
Dimensional verification — every batch is inspected; functional sampling on pieces tested for fatigue and fracture.
Mechanical testing — ISO 14801:2016 fatigue and accelerated-ageing testing under cyclic loads representative of the oral environment.
Biocompatibility validation — cytotoxicity (ISO 10993-5:2009) and intracutaneous testing / irritation (ISO 10993-10:2021), following ISO 10993-1:2025 principles.
Service-life guarantee — IBO's quality commitment ensures durability and performance across the device's service life.
Product description last updated: May 19, 2026

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