IBO Odontit - IBO - LOCK-ATTACH Hard White Retention Set 5 lbs (5 u) - Poliamide66 - # HE-41915 ( WORKFLOW )

IBO Odontit - IBO - LOCK-ATTACH Hard White Retention Set 5 lbs (5 u) - Poliamide66 - # HE-41915    ( WORKFLOW )
SKU: 483841 - IN STOCK
$25.20
Quantity:

Minimum quantity is 1.

Manufacturer #
HE-41915
Manufacturer
Model
Lock-Attach
SubModel
Silicones
Style
Silicones
Length
4.8mm
5 in Stock & Selling

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Description

IBO
Connections that Transform

LOCK-ATTACH Retention Insert — Hard White (Strong Retention, HE-41915)

Reference HE-41915 · IBO LOCK-ATTACH Retention insert · Hard White colour-coded · Strong Retention
LOCK-ATTACH Retention Insert — Hard White (Strong retention, HE-41915) — product photo

DESCRIPTION

IBO manufactures the Hard White silicone Retention insert for the LOCK-ATTACH overdenture attachment system. The Hard White insert provides a strong Retention Retention level: higher Retention force for patients who have adapted to overdenture wear and require firmer Retention.

The Retention insert sits inside the LOCK-ATTACH Titanium Female Housing (HE-41918) embedded in the overdenture base and engages the male LOCK-ATTACH Abutment screwed onto the implant. Insert colour is the only way to identify Retention class chairside.

Retention class: Strong Retention.
Colour code: Hard White.
Material: medical-grade silicone validated for intra-oral use.
Function: snap-fit Retention element inside the LOCK-ATTACH titanium female housing.
Indication: tune overdenture Retention force per patient need and rehabilitation phase.
Maintenance: replaceable wear component; periodic replacement is normal for overdenture maintenance.

CLINICAL APPLICATION

The Hard White insert is selected when the prosthodontist requires strong Retention Retention — either to compensate for limited manual dexterity in the patient, to stage Retention over the rehabilitation timeline, or to balance Retention across multiple LOCK-ATTACH abutments in the same arch.

A common protocol is to start a new overdenture with a lower Retention class while the patient learns to seat and remove the prosthesis, then step up to higher Retention as the patient adapts.

Chairside swap: remove the worn insert from the titanium housing and snap in the replacement.
Mixed Retention classes within the same arch are common — different abutment positions may use different inserts.
Service life: depends on patient use; periodic inspection at recall is standard.

PLATFORM & COMPATIBILITY

This Retention insert is a wear component within the IBO LOCK-ATTACH overdenture attachment system. It is compatible across all LOCK-ATTACH platforms (Internal Hex, Conical Reactive, Multiunit) since the female housing is platform-agnostic.

Component layerReference
Implant-side male abutmentHEI-359xx / HEC-359xx / HEC-439xx / HE-48903 series
Female housing (overdenture-side)HE-41918 (Titanium Female Housing)
This Retention insertHE-41915 (Hard White, Strong Retention)
Other Retention classes availableHE-41913 (Soft Blue), HE-41914 (Medium Pink), HE-41915 (Hard White), HE-41916 (Soft Red), HE-41917 (Black)

TECHNICAL SPECIFICATIONS

Manufacturer referenceHE-41915
BrandIBO
Product familyLOCK-ATTACH Retention Insert
Component roleWear / Retention element (overdenture-side)
Retention classStrong Retention
Colour codeHard White
MaterialMedical-grade silicone
CompatibilityAll LOCK-ATTACH platforms via HE-41918 female housing
RegulatoryCE marking MDR · ISO 13485:2016 · AEMPS licence

MATERIALS & SURFACE

IBO LOCK-ATTACH Retention inserts are manufactured from medical-grade silicone formulations validated for intra-oral use. Each Retention class is colour-coded for fast chairside identification.

The silicone formulation provides controlled, repeatable Retention force across the service life of the insert and is designed for periodic replacement as part of routine overdenture maintenance.

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

STERILIZATION & HANDLING

IBO LOCK-ATTACH 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 component geometry or surface in any way; doing so compromises 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 component carries the CE marking MDR, assessed by a Notified Body.

Five quality foundations apply to this component:

Material selection — alloys and silicones validated for biocompatibility and durability.
Dimensional verification — every batch is inspected; functional sampling on pieces tested for fatigue.
Mechanical testing — ISO 14801:2016 fatigue 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

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