IBO - Open Tray Impression Coping + Screw - Straumann Bone Level RC Titanium. Inox - # HI-41700 - # HI-41700

IBO - Open Tray Impression Coping + Screw - Straumann Bone Level RC Titanium. Inox - # HI-41700 - # HI-41700
SKU: 494354 - IN STOCK | 5 in Stock & Selling
$31.98
Quantity:

Minimum quantity is 1.

Manufacturer #
HI-41700
Manufacturer
Model
STRAUMANN
SubModel
Bone Level
Features
Imp Copings
Features
Regular CrossFit
Features
Titanium
Package
1pk
5 in Stock & Selling
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Description

ODONTIT
Connections that Transform

Open Tray Impression Coping — Straumann® Bone Level RC

Reference HI-41700 · ODONTIT IBO prosthetic line · RC platform
Product photography available on request
HI-41700

DESCRIPTION

ODONTIT manufactures this open tray impression coping for restorative cases that follow the Straumann® Bone Level CrossFit® prosthetic protocol. The open tray (pick-up) impression coping transfers the exact three-dimensional implant position to the master cast, and is retained in the impression material when the tray is removed. Every component is machined to the connection tolerances of the original platform and supplied in the manufacturer’s validated condition for clinical use.

This reference, HI-41700, is supplied for the Regular CrossFit (RC) platform.

Component family: Open Tray Impression Coping.
Platform: Regular CrossFit (RC).
Material: Ti-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3) with stainless steel (Inox) fixing scre.
Connection: CrossFit® RC — machined to the original prosthetic interface.
Supplied as: 1pk — single component, single patient, single procedure.

CLINICAL APPLICATION

Regular CrossFit (RC) — the regular prosthetic platform of the Straumann® Bone Level system.

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.

Indicated for open tray (pick-up) implant-level impressions.
Verify full seating radiographically before injecting impression material.
Splint adjacent copings for multi-unit cases to control distortion.

PLATFORM & COMPATIBILITY

This component is positioned as informational compatibility with the Straumann® Bone Level Regular CrossFit (RC) connection. ODONTIT supplies independent compatible prosthetic components; final clinical use must be verified against the implant manufacturer’s documentation.

System referencePlatformODONTIT equivalent
Straumann® Bone Level (informational)RCOpen Tray Impression Coping RC
Straumann® Bone Level Tapered (informational)RCOpen Tray Impression Coping RC
ODONTIT prosthetic lineRCFull RC component series

Straumann®, Bone Level® and CrossFit® are trademarks of their respective owners. ODONTIT is an independent manufacturer with no affiliation, sponsorship or endorsement from the listed brands.

TECHNICAL SPECIFICATIONS

Manufacturer referenceHI-41700
BrandODONTIT
Product familyOpen Tray Impression Coping
PlatformRegular CrossFit (RC)
Connection typeCrossFit® RC
MaterialTi-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3) with stainless steel (Inox) fixing scre
Compatibility (informational)Straumann® Bone Level RC
Package1pk
RegulatoryCE marking MDR · ISO 13485:2016 · AEMPS licence

MATERIALS & SURFACE

ODONTIT 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. All materials and processes comply with current regulations and are subject to full traceability from raw material to final validation.

STERILIZATION & HANDLING

ODONTIT components are supplied in the manufacturer’s validated condition for clinical use. Follow the package insert and the ODONTIT Instructions for Use for handling, storage and any chairside preparation steps. Do not modify the component 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 components per local biohazard regulations.

QUALITY ASSURANCE

ODONTIT 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 ODONTIT component carries the CE marking MDR, assessed by a Notified Body.

Five quality foundations apply to this component:

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 — ODONTIT’s quality commitment ensures durability and performance across the device’s service life.
Product description last updated: August 13, 2026

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