Bond Apatite Bone Graft Cement 1cc

Augma Bond Apatite™ Bone Graft Cement 1cc

Intended Use

Augma Bond Apatite™ is a composite bone graft cement intended for filling, reconstruction, and augmentation of osseous defects in the oral and maxillofacial region. The material is designed to provide long-term space maintenance and support predictable bone regeneration in preparation for future implant placement and restorative procedures.

The graft consists of a biphasic calcium sulfate cement matrix combined with hydroxyapatite (HA) granules, creating a stable scaffold for bone formation and defect preservation.

Indications

Bond Apatite™ is indicated for:

- Socket preservation following tooth extraction.
- Socket grafting with flap reflection.
- Socket grafting without flap reflection.
- Extraction sockets with compromised bony walls.
- Lateral ridge augmentation.
- Horizontal ridge augmentation.
- Bone augmentation in the aesthetic zone.
- Open sinus lift procedures.
- Closed sinus lift procedures.
- Implant site development.
- Localized alveolar bone defects.

Contraindications

Do not use:

- In patients with known hypersensitivity to any component of the material.
- In active untreated infections.
- In sites with inadequate vascular supply.
- In situations where bone grafting is contraindicated.

Warnings

- For professional dental use only.
- Use aseptic surgical technique.
- Do not use damaged or expired products.
- Single-use device. Do not resterilize or reuse.
- Ensure complete debridement of the surgical site before graft placement.

Precautions

- Follow standard surgical and implantology protocols.
- Avoid contamination of the graft material.
- Ensure adequate stabilization of the grafted site.
- Protect the graft from excessive mechanical forces during healing.
- Follow postoperative instructions carefully.

Instructions for Use

1. Site Preparation
  - Prepare the surgical site according to the planned augmentation procedure.
  - Remove all granulation tissue and pathological tissue.
  - Thoroughly debride the defect.
  - Irrigate with sterile saline solution.
  - Achieve adequate bleeding from the recipient site when clinically appropriate.

2. Material Preparation
  - Open the package using sterile technique.
  - Prepare Bond Apatite™ according to the manufacturer's instructions.
  - Ensure proper consistency before placement.

3. Graft Placement

  - Place Bond Apatite™ directly into the osseous defect.
  - Adapt and condense the material to completely fill the defect.
  - Shape the graft to reproduce the desired ridge contour and volume.
  - Avoid excessive compression that could compromise blood supply.
  - Verify complete adaptation of the material to the defect walls.

4. Socket Preservation Procedure
  - Following extraction and socket debridement, place Bond Apatite™ into the socket.
  - Fill the socket to the desired level.
  - Adapt the material carefully to maintain ridge dimensions.
  - Manage soft tissues according to the selected clinical protocol.

5. Ridge Augmentation Procedure
  - Prepare the recipient site.
  - Place and contour the graft material to achieve the desired ridge width and volume.
  - Stabilize the graft according to the clinician's preferred surgical protocol.
  - Achieve soft tissue closure when indicated.

6. Sinus Augmentation Procedure
  - Prepare the sinus according to accepted surgical techniques.
  - Carefully place Bond Apatite™ into the elevated sinus cavity.
  - Avoid overpacking the material.
  - Complete the procedure according to the selected sinus augmentation protocol.

7. Soft Tissue Management
  - Follow the surgical protocol appropriate for the procedure performed.
  - Primary closure may be achieved when clinically indicated.
  - Ensure adequate protection of the grafted site during healing.

8. Healing Phase
  - Bond Apatite™ functions as a long-term space-maintaining scaffold.
  - The biphasic calcium sulfate component gradually resorbs during healing.
  - Hydroxyapatite particles contribute to long-term volume stability.
  - Progressive replacement with newly formed bone occurs over time.
  - Healing times may vary depending on defect size, patient factors, and surgical technique.

9. Postoperative Care
  - Follow standard postoperative protocols.
  - Advise the patient to avoid trauma to the grafted site.
  - Maintain proper oral hygiene.
  - Schedule periodic clinical evaluations.
  - Evaluate healing before implant placement or restorative treatment.

Storage

Store in the original packaging in a cool, dry environment protected from direct sunlight, excessive heat, and moisture.
Do not use after the expiration date.

Disposal

Dispose of unused material and packaging according to local regulations and clinical waste management protocols.
Professional Use Only
This product is intended for use by qualified dental professionals trained in oral surgery, implantology, and regenerative procedures.