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Product Description
Titanium Base 0.5 Round for Narrow Implant H2.1
Titanium Base 0.5 Round for Narrow Implant H2.1 is a prosthetic component designed for the fabrication of custom implant-supported restorations using digital CAD/CAM workflows. Its round profile provides a titanium interface between the compatible implant and the custom restorative component.
Designed for the narrow implant platform, this titanium base supports restorative planning in areas with limited prosthetic space. The Internal Hex H2.1 connection interfaces with compatible narrow implants, supporting accurate positioning and fixation of the restoration.
Manufactured from titanium, the component combines strength, bio-compatibility, and corrosion resistance for implant prosthetic applications.
Key Features
- Designed for digital CAD/CAM restorative workflows
- Round-profile titanium base
- Narrow platform for compatible H2.1 implants
- Internal Hex H2.1 implant connection
- Strong, biocompatible, and corrosion-resistant titanium
- Provides a foundation for compatible custom restorations
Indications & Applications
Titanium Base 0.5 Round for Narrow Implant H2.1 is intended for:
- Fabrication of custom implant-supported restorations
- Digital CAD/CAM laboratory workflows
- Restorative applications involving compatible narrow H2.1 implants
- Cases with limited prosthetic space, subject to clinical assessment
Use for single-unit or multi-unit restorations must follow the indications for the specific titanium base and its engaging or non-engaging design.
Clinical Benefits
- Supports precise positioning of compatible restorative components
- Provides a titanium interface at the implant connection
- Supports custom restoration design and emergence-profile planning
- Integrates into compatible digital laboratory workflows
Sterilization & Handling
- Follow the manufacturer’s instructions for cleaning and sterilization before clinical use
- Confirm implant, fixation screw, and restoration compatibility
- Use the manufacturer-specified tightening torque
- Follow the prescribed bonding and handling protocol for the selected restorative material
Advantages
- Round profile for custom restorative applications
- Titanium construction with corrosion resistance
- Designed for the narrow H2.1 implant platform
- Supports coordinated laboratory and clinical workflows
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Titanium Base 0.5 Round for Narrow Implant H2.1
Intended Use
The Titanium Base 0.5 Round serves as an interface between a compatible narrow H2.1 implant and a custom prosthetic restoration. Use only within the indications approved by the manufacturer for this specific component.
For use by qualified dental professionals and trained dental laboratory personnel.
Compatibility
Before use, confirm the exact implant platform, titanium base, fixation screw, driver, and digital library compatibility. An H2.1 connection designation alone does not establish compatibility with every implant system.
Confirm whether the component is engaging or non-engaging and whether it is approved for the planned single-unit or splinted restoration.
Preparation Before Use
- Inspect the packaging, product identification, and component for damage.
- Do not use a component with visible deformation, damaged threads, or a damaged connection surface.
- Verify the supplied sterile or non-sterile status on the product label.
- Process the component according to its manufacturer-validated cleaning and sterilization instructions before clinical use.
Laboratory Procedure
- Select the correct digital library and restorative components for the exact titanium base.
- Design and fabricate the restoration within the manufacturer’s specified dimensions and material limitations.
- Preserve the implant connection, screw seat, and screw channel. Do not modify these surfaces.
- Where bonding is indicated, follow the approved surface-treatment and bonding instructions for the titanium base, restorative material, and bonding agent.
- Remove excess bonding material and inspect the completed restoration for fit and unobstructed screw access.
- Follow validated processing instructions for the completed restoration before clinical placement.
Clinical Placement
- Inspect and clean the implant connection according to the implant manufacturer’s instructions.
- Position the restoration and verify complete seating without forcing the component.
- Use only the specified fixation screw and compatible driver.
- Tighten with a calibrated torque instrument to the manufacturer’s prescribed torque for this exact component and screw.
- Verify seating, stability, proximal contacts, and occlusion.
- Complete screw-access closure according to the approved restorative protocol.
Cleaning and Sterilization
Use only the manufacturer’s validated processing procedure. This must specify the cleaning method, sterilization method, cycle temperature, exposure time, and drying requirements.
Confirm that the selected procedure is compatible with the entire assembled restoration, including any bonding materials. A temperature alone is not a complete sterilization protocol.
Warnings and Precautions
- Secure small components against accidental swallowing or aspiration.
- Do not use incompatible components or exceed the specified tightening torque.
- Do not use in patients with a known hypersensitivity to the component’s materials.
- Follow the product labeling regarding single use and reuse restrictions.
- If complete seating or stable fixation cannot be achieved, identify and resolve the cause before completing treatment.
