Titanium Screw for Esthetic Multi Unit M1.6

Titanium Screw for Esthetic Multi Unit M1.6

General Information

Before using DMi products, the dentist, maxillofacial surgeon, or dental technician should carefully read the indications, contraindications, recommendations, warnings, and instructions, as well as all additional product information, including product descriptions, surgical and prosthetic manuals, catalogs, and related documentation.
DMi also recommends participation in relevant continuing education courses conducted on-site or remotely by authorized DMi specialists.
Detailed documentation and training information are available through authorized DMi representatives and on the company website:
www.dmimplant.online

Product Description

The Titanium Screw for Esthetic Multi Unit M1.6 is intended for fixation of prosthetic components to esthetic multi-unit abutments in implant-supported restorations.
The screw is manufactured from high-quality medical-grade titanium alloy and is designed to provide stable mechanical fixation, accurate prosthetic positioning, and long-term restorative stability.

Technical Specifications

- Product type: Prosthetic fixation screw
- Thread type: M1.6
- Material: Medical-grade titanium alloy
- Application: Esthetic multi-unit prosthetic fixation

The screw is compatible with:

- Esthetic multi-unit abutments
- Screw-retained restorations
- Full-arch restorations
- Temporary restorations
- Permanent restorations
- Laboratory restorative procedures

The component is installed using the appropriate prosthetic driver according to the recommended torque protocol.

Warnings

- The product is intended for single-patient use only.
- The product is supplied non-sterile unless otherwise indicated.
- Sterilization in an autoclave at 135°C (275°F) before clinical use is recommended.
- Excessive tightening torque may damage the screw or prosthetic components.
- Insufficient torque may result in screw loosening or prosthetic instability.
- The dentist or dental technician must be familiar with implant prosthetic procedures and torque protocols.

Indications

The Titanium Screw M1.6 is intended for securing prosthetic components to esthetic multi-unit abutments in implant-supported restorations.

Suitable for:

- Screw-retained restorations
- Full-arch restorations
- Multi-unit restorations
- Temporary prosthetics
- Permanent prosthetics
- Laboratory procedures

Contraindications

- Lack of implant osseointegration
- Allergy or hypersensitivity to titanium alloy
- Use with incompatible prosthetic components
- Insufficient implant stability

Procedure for Use

Clinical Procedure

1. Verify compatibility of the prosthetic component and esthetic multi-unit abutment.
2. Clean and dry all prosthetic connection surfaces before installation.
3. Position the prosthetic restoration onto the esthetic multi-unit abutment.
5. Insert the Titanium Screw M1.6 through the prosthetic structure into the abutment connection.
6. Tighten the screw using the appropriate prosthetic driver according to the recommended clinical torque value.
7. Verify passive seating and stability of the prosthetic restoration.
8. For definitive restorations, retightening after initial loading may be recommended according to the clinical protocol.
9. Periodic clinical follow-up is recommended to evaluate prosthetic stability and screw integrity.

Sterilization

- The product is supplied non-sterile unless otherwise indicated and must be sterilized before use in an autoclave at: 135°C (275°F)
- Single-patient use only.

Storage

Store in a clean, dry environment at room temperature away from direct sunlight, moisture, and contamination.

Disclaimer

DMi, the importer and supplier of DMi products, is not responsible for complications, injuries, or other negative consequences resulting from:

- Incorrect clinical indications
- Improper prosthetic technique
- Incorrect component selection
- Improper torque application
- Improper use or handling of instruments and components
- Failure to follow the instructions for use

The treating dentist, maxillofacial surgeon, and dental technician are solely responsible for appropriate clinical and laboratory application of the product.
DMi recommends appropriate professional training and participation in specialized DMi educational programs prior to use.

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