IBO Odontit - IBO - Closed Tray Impression Transfer Coping + Screw Multiunit RP Stainless Steel - # HE-48710 ( WORKFLOW )

IBO Odontit - IBO - Closed Tray Impression Transfer Coping + Screw Multiunit RP Stainless Steel - # HE-48710  ( WORKFLOW )
SKU: 483829 - IN STOCK
$27.96
Quantity:

Minimum quantity is 1.

Manufacturer #
HE-48710
Manufacturer
Model
Multiunit
SubModel
Impression Copyng
Features
WORKFLOW
Diameter
Multiunit RP
Length
4.8mm
5 in Stock & Selling

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Description

IBO
Connections that Transform

Closed Tray Imp HE-48710

Reference HE-48710 · IBO Closed-Tray Impression Coping · Transfer-pin workflow
Closed Tray Imp HE-48710 — product photo

DESCRIPTION

IBO Closed-Tray Impression Coping for conventional Impression workflows, reference HE-48710, Closed Tray Imp HE-48710. Used with a standard (non-perforated, Closed) Impression Tray; the Coping remains on the implant when the Tray is removed and is then transferred to the Impression for analog mounting in the laboratory.

Reference: HE-48710 · Closed Tray Imp HE-48710.
Workflow: Closed-Tray Transfer ImpressionCoping remains in mouth when Tray is removed.
Material: medical-grade titanium alloy with platform-specific geometry for re-seating in Impression.
Retention features: anti-rotation flats / grooves engaging the Impression material.
Single use during the Impression visit.
Lower-cost simpler workflow vs. open-Tray — preferred for single-implant cases.

CLINICAL APPLICATION

Used at the Impression visit in conventional analog workflows for single-implant or simple cases where a fully passive multi-unit master model is not required. The Coping is screwed onto the implant, the Closed-Tray Impression is taken, the Tray is removed leaving the Coping in the mouth, the Coping is then unscrewed and re-seated into the Impression material for laboratory analog mounting.

Workflow: place Coping → fixate → Closed-Tray Impression → remove Tray → unscrew Coping → re-seat Coping into Impression void → ship to lab.
Indication: single-implant cases, or where open-Tray access is anatomically restricted.
Compatible with polyether or VPS Impression material.
For multi-unit or full-arch cases, prefer open-Tray for higher accuracy.

PLATFORM & COMPATIBILITY

Used with IBO implant platforms per the MFG# prefix (HEI / HEC / HE). Confirm platform pairing via the IBO catalogue.

TECHNICAL SPECIFICATIONS

Manufacturer referenceHE-48710
BrandIBO
Product familyClosed-Tray Impression Coping
DesignationClosed Tray Imp HE-48710
WorkflowConventional / analog Closed-Tray Transfer-pin Impression
MaterialTi-6Al-4V ELI Grade 5
CompatibilityIBO Conical Reactive + Multiunit platforms — per MFG# prefix
RegulatoryCE marking MDR · ISO 13485:2016 · AEMPS licence

MATERIALS & SURFACE

Machined from medical-grade Ti-6Al-4V ELI titanium (Grade 5), ASTM F136 / ISO 5832-3, selected for biocompatibility, mechanical strength and chemical stability in the oral environment.

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

STERILIZATION & HANDLING

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 geometry or surface in any way; doing so compromises both clinical fit and 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.

Material selection — alloys validated for biocompatibility and durability.
Dimensional verification — every batch inspected; functional sampling under fatigue and fracture testing.
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 (ISO 10993-10:2021), following ISO 10993-1:2025 principles.
Service-life guaranteeIBO quality commitment ensures durability and performance across the device's service life.
Product description last updated: May 19, 2026

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