Titanium Base - 10mm For Esthetic Multi-Unit M1.6

Titanium Base 10 mm for Esthetic Multi-Unit M1.6

Intended Use

The Titanium Base 10 mm for Esthetic Multi-Unit M1.6 is a prosthetic component intended to provide an interface between a compatible esthetic multi-unit abutment and a custom dental restoration, within the manufacturer’s approved indications.

For use by qualified dental professionals and trained dental laboratory personnel.

Compatibility & Component Selection

- Confirm compatibility with the exact esthetic multi-unit abutment platform.
- Use only the fixation screw and driver specified for this titanium base.
- The M1.6 designation alone does not establish compatibility with other systems.
- Confirm the approved restoration type and whether the component is engaging or non-engaging before treatment planning.
- Do not connect the titanium base directly to an implant unless expressly permitted by the manufacturer.

Laboratory Procedure

- Verify the fit of the titanium base on the specified multi-unit analog or compatible abutment.
- Select the appropriate restorative workflow and, where applicable, the digital library for the exact component.
- Fabricate the restoration within the approved material, dimensional, and design limits.
- Modify the base only where explicitly permitted by the manufacturer. Preserve the connection surface, screw seat, and screw channel.
- Where bonding is indicated, follow the validated surface-treatment and bonding protocols for the titanium base, restoration, and bonding agent.
- Remove excess bonding material and verify that the screw channel and connection surfaces remain clear.
- Inspect the completed restoration for fit and process it according to the validated instructions before clinical placement.

Clinical Placement

- Inspect the multi-unit abutment interface and remove debris according to the system instructions.
- Position the completed restoration and confirm complete seating without force.
- For splinted restorations, verify passive fit before final tightening.
- Insert the specified prosthetic fixation screw using the appropriate driver.
- Tighten with a calibrated torque instrument to the manufacturer’s prescribed torque for this exact base and screw combination.
- Verify seating, stability, occlusion, and proximal contacts; use radiographic assessment when clinically indicated.
- Complete screw-access closure according to the approved restorative protocol.

Cleaning & Sterilization

- Follow the manufacturer’s validated instructions for cleaning, disinfection, packaging, sterilization, and drying.
- The sterilization procedure must specify the cycle type, temperature, exposure time, and drying requirements. Confirm compatibility with all materials in the completed restoration, including bonding agents.
- Do not apply a sterilization protocol from another component without confirmation.

Warnings & Precautions

- Secure small components against swallowing or aspiration.
- Do not force an incompletely seated restoration into position by tightening the screw.
- Do not exceed the specified tightening torque.
- Do not use in patients with known hypersensitivity to the component’s materials.
- Follow product labeling concerning single use and reuse restrictions.
- If fit or fixation is unsatisfactory, identify and resolve the cause before completing treatment.