ODONTIT manufactures this healing cap for restorative cases that follow the Straumann® Bone Level CrossFit® prosthetic protocol. The healing cap seals and shapes the peri-implant soft tissue during the healing phase and protects the internal connection from bone and tissue ingrowth. 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-41402, is supplied for the Regular CrossFit (RC) platform at a 2mm gingival height.

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.

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.

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.

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.

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.

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: