IBO - M1.8 Healing Cap height 4mm - INTHEX NP (3.5mm) NP. Titanium - # HEI-35404
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Description
M1.8 Healing Cap HEI-35404
DESCRIPTION
IBO Healing Cap, reference HEI-35404, M1.8 Healing Cap HEI-35404. Designed to protect the implant connection and maintain gingival contour during the soft-tissue Healing phase of two-stage implant protocols at the Internal Hex (INTHEX) / matched-platform platform.
CLINICAL APPLICATION
Used during the soft-tissue Healing phase for IBO Internal Hex (HEI) platform implant fixtures.
PLATFORM & COMPATIBILITY
Used with IBO implant fixtures at the Internal Hex (INTHEX) / matched-platform platform. The threaded interface matches the corresponding implant fixture's Healing-Cap seat; consult the IBO Conical Reactive platform reference (Ø3.0 / NP / RP / WP) to confirm pairing.
TECHNICAL SPECIFICATIONS
| Manufacturer reference | HEI-35404 |
|---|---|
| Brand | IBO |
| Product family | Healing Cap |
| Designation | M1.8 Healing Cap HEI-35404 |
| Platform | Internal Hex (INTHEX) / matched-platform |
| Material | Ti-6Al-4V ELI Grade 5 (ASTM F136 / ISO 5832-3) |
| Compatibility | IBO Conical Reactive Internal Hex (INTHEX) / matched-platform implant fixtures |
| Package | 1pk |
| Regulatory | CE 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.