IBO Odontit - IBO -Conical Active RP ( 4.3mm ) WP ( 5.0mm ) Implant Analogue + Fixing Screw for digital Use - # HEC-43300

IBO Odontit - IBO -Conical Active RP ( 4.3mm ) WP ( 5.0mm ) Implant Analogue + Fixing Screw for digital Use - # HEC-43300
SKU: 483748
Quantity:

Minimum quantity is 1.

Manufacturer #
HEC-43300
Manufacturer
Model
CONICAL
Features
Implant Fixtures
Package
1pk
ETD
Unavailable

Description

IBO
Connections that Transform

Conical Multiunit Mini Abutment — RP (Ø4.3)

Reference HEC-43300 · IBO Conical Active line · for multi-Implant prosthetic rehabilitation
Conical Multiunit Mini Abutment — RP (Ø4.3) — product photo

DESCRIPTION

IBO manufactures the Conical Multiunit Mini Abutment for prosthetically-driven multi-Implant rehabilitations on the IBO Conical Reactive platform. This reference, HEC-43300, mounts on the IBO Conical RP platform (Regular Platform, Ø4.3 class) and provides a multiunit prosthetic interface for Screw-retained bars, bridges and overdentures.

The Multiunit Mini Abutment is designed for arch-level rehabilitations, including All-on-4®-style protocols, Screw-retained bridgework and immediate-loading scenarios when the surgical team selects an immediate-loading prosthetic workflow.

Platform: RP (Regular Platform) on the IBO Conical Reactive line.
Host Implant compatibility: IBO Reactive fixtures in the RA43xx (Ø4.3 mm Reactive fixtures) series.
Function: Multiunit prosthetic interface — converts the Implant's conical seat into a standardized multiunit prosthetic platform.
Indications: Screw-retained bars / bridges / overdentures, multi-Implant rehabilitations.
Material: medical-grade Ti-6Al-4V ELI titanium (Grade 5), ASTM F136 / ISO 5832-3.
System compatibility (informational): Nobel Biocare® NOBEL Active® Ø4.3 protocol.

CLINICAL APPLICATION

The RP Multiunit Mini Abutment is selected when the prosthetic plan calls for an angle-correction or arch-level multiunit interface above the Implant body. It standardizes the prosthetic platform across implants of differing platforms and angulations, simplifying impression-taking, framework design and prosthetic loading.

Final indication, abutment height and angulation selection must be determined by the treating prosthodontist based on the prosthetic plan.

Workflow: open-tray or closed-tray impression at the multiunit level; framework verification on multiunit analogues.
Loading: follows IBO loading protocol; immediate loading per case-specific primary stability and prosthetic-plan assessment.
Hygiene: machined cuff designed for soft-tissue compatibility at the prosthetic emergence.

PLATFORM & COMPATIBILITY

The Conical RP Multiunit Mini Abutment (Ø4.3 class) is positioned as informational compatibility with the Nobel Biocare® NOBEL Active® Ø4.3 multiunit protocol. IBO supplies independent compatible prosthetic components; final clinical Use must be verified against the Implant manufacturer's documentation.

Component layerReference
Host Implant body (IBO Reactive)RA43xx (Ø4.3 mm Reactive fixtures)
This Multiunit Mini AbutmentHEC-43300
Compatible system (informational)Nobel Biocare® NOBEL Active® Ø4.3

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 referenceHEC-43300
BrandIBO
Product familyConical Multiunit Mini Abutment
PlatformRP (Regular Platform, Ø4.3 class)
FunctionMultiunit prosthetic interface
IndicationScrew-retained bars / bridges / overdentures
MaterialTi-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3)
Host Implant series (IBO)RA43xx (Ø4.3 mm Reactive fixtures)
Compatibility (informational)Nobel Biocare® NOBEL Active® Ø4.3
Package1pk
RegulatoryCE marking MDR · ISO 13485:2016 · AEMPS licence

MATERIALS & SURFACE

IBO Multiunit Mini Abutments are machined from medical-grade Ti-6Al-4V ELI titanium, Grade 5, 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.

The component is finished with a polished, machined surface at the gingival/prosthetic interface for soft-tissue health, and a machined connection seat machined to the IBO Conical platform tolerances.

All materials and processes are subject to full traceability from raw material to final validation.

STERILIZATION & HANDLING

IBO abutment components are supplied in the manufacturer's validated condition for clinical Use. Follow the package insert and IBO Instructions for Use for handling, storage and torque protocol. Do not modify the abutment geometry 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 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 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 guaranteeIBO's quality commitment ensures durability and performance across the device's service life.
Product description last updated: May 19, 2026

Attachments