IBO - Implant Fixture 3.5D x 8mm INTHEX NP (3.5mm) - Roughed & Etched surface - # SGI3508

IBO  - Implant Fixture 3.5D x 8mm INTHEX NP (3.5mm) - Roughed & Etched surface - # SGI3508
IBO  - Implant Fixture 3.5D x 8mm INTHEX NP (3.5mm) - Roughed & Etched surface - # SGI3508
SKU: 483036 - In stock
Quantity:

Minimum quantity is 1.

Manufacturer #
SGI3508
Manufacturer
Model
ZIMMER
Features
Implant Fixtures
Package
1pk
In Stock
15

Description

ODONTIT
Connections that Transform

Internal Hex Implant Fixture — Ø3.5 mm × 8mm

Reference SGI3508 · ODONTIT INTHEX line · Internal Hex NP platform · Self-tapping
Internal Hex Implant Fixture — Ø3.5 mm × 8mm — product photo

DESCRIPTION

ODONTIT manufactures the INTHEX (Internal Hex) Implant Fixture line for restorative cases that follow the Zimmer® internal-hex prosthetic protocol. The Ø3.5 mm Fixture is engineered with a self-tapping apical thread profile and 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, SGI3508, delivers a Ø3.5 mm body × 8mm length, with the IBO Internal Hex prosthetic connection in the NP platform.

Body diameter: Ø3.5 mm.
Body length: 8mm.
Platform: NP (Narrow Platform).
Connection: Internal Hex — proven prosthetic interface with broad component availability.
Apical design: self-tapping thread profile for primary stability across a range of bone qualities.
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: Zimmer®-compatible Internal Hex (informational) — Ø3.5 class.

CLINICAL APPLICATION

The Ø3.5 mm INTHEX Fixture at the NP class is intended for restorative scenarios requiring a narrow prosthetic emergence on the Internal Hex protocol — including lateral incisor sites, lower incisor regions and reduced-ridge scenarios.

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.

Restorative indication: matches the corresponding Zimmer® Internal Hex prosthetic protocol class.
Prosthetic loading: per IBO loading protocol and ISO 14801:2016 testing envelope.
Recommended workflow: pair with IBO Internal Hex abutments designed for the NP platform and Zimmer®-protocol prosthetic components.
Hex driver and torque control must follow Internal Hex platform standards.

PLATFORM & COMPATIBILITY

The Internal Hex NP connection (Ø3.5 mm) is positioned as informational compatibility with the Zimmer Dental® Internal Hex Ø3.5 system. IBO supplies independent compatible prosthetic components; final clinical use must be verified against the Implant manufacturer's documentation.

System referencePlatformIBO INTHEX equivalent
Zimmer Dental® Internal Hex (informational)Ø3.5INTHEX NP (Ø3.5 class)
IBO Abutment lineNPIBO Internal Hex prosthetic series for the NP platform

Zimmer® and Zimmer Dental® 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 referenceSGI3508
BrandODONTIT
Product familyInternal Hex Implant Fixture (INTHEX)
DiameterØ3.5 mm
Length8mm
PlatformNP (Narrow Platform)
Connection typeInternal Hex
Thread designSelf-tapping
surface treatmentRoughened and Etched
Body materialTi-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3)
Compatibility (informational)Zimmer Dental® Internal Hex Ø3.5
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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