maxgraft® bonering

SIMULTANEOUS BONE AUGMENTATION AND IMPLANT PLACEMENT

patient comfort

SHORTER TREATMENT TIMES

One-stage procedure

maxgraft® bonering is a prefabricated cancellous ring made from processed human donor bone. maxgraft® bonering enables the implant placement and bone augmentation in one step1 .

FAST RECONSTRUCTION OF BONE

With the Bone Ring Technique, the treatment time can be shortened by several months, as a second operation for implant placement is avoided. The bony integration of the bone ring and the implant takes place over the surrounding vital bone. After a six-month healing period, reopening and prosthetic restoration can take place. The use of an allogenic bone ring instead of the patient’s own bone can increase patient comfort. The risks associated with autogenous bone harvesting, such as donor site morbidity, increased risk of infection and postoperative pain, can be avoided or prevented1,2.

HIGH PATIENT ACCEPTANCE – SHORTER TREATMENT TIMES

Due to its high biological regenerative capacity and complete remodeling, maxgraft® represents an alternative to the patient’s own bone. The need for a second surgical site is eliminated, surgical time is shortened, and postoperative pain and morbidity for the patient are significantly reduced.

Product Specifications

maxgraft® bonering 3.3

Recommended for implant diameters from 3.3 – 3.5 mm

Art.-No. Dimension Content
33160 cancellous ring, ø 6 mm, height 10 mm

1 x
33170 cancellous ring, ø 7 mm, height 10 mm

1 x

maxgraft® bonering 4.1

Recommended for implant diameters from 4.1 – 4.5 mm

Art.-No. Dimension Content
33174 cancellous ring, ø 7 mm, height 10 mm

 

1 x

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SPECIFIC FACTS

Simultaneous implant placement through the maxgraft® bonering provides primary stability of the implant and ring in the local bone. The ring technique shortens the treatment time and avoids the second implantation procedure and reduces patients morbidity.

The production process of maxgraft® preserves the natural collagen and a residual moisture of <10%. Nevertheless, it is recommended to rehydrate maxgraft® bonering before use (10 min in saline solution). Rehydration in saline solution leads to improved flexibility of the ring (especially for the 7 mm ring), therefore it is less prone to fracture and can be more easily adapted to the defect area.

maxgraft® is processed bone substitute material from human donors. maxgraft® bonering is milled from cancellous bone blocks by C+TBA. The blocks originate from femoral heads of living donors donated during hip arthroplasty surgery. Procurement is standardized according to a predefined protocol and is performed by certified procurement centers. All tissue donations are made only after the donor has given written consent. In addition, the health status of each potential donor is assessed in advance as part of a risk analysis and the donor is then selected on the basis of strict exclusion criteria.

After a thorough analysis of the donors’ medical history, the high safety of maxgraft® is ensured by a series of rigorous serological tests in combination with the Allotec® purification process of the C+TBA and final radiological sterilization.
C+TBA is certified as a tissue procurement facility and tissue bank according to §19 and §22 of the Austrian Tissue Safety Act.

Guide Bone substitute materials

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PRODUCTOS RELACIONADOS

  • maxgraft® bonering surgical kit

    All necessary instruments for maxgraft® bonering

    With this surgical kit, botiss biomaterials provides all necessary instruments to apply the maxgraft® bonering.

  • Jason® membrane

    NATIVE PERICARDIUM MEMBRANE FOR GBR/GTR

    A native collagen membrane obtained from porcine pericardium, offering multi-directional strength and tear resistance.

  • cerabone®

    100% PURE BONE MINERAL

    a 100% pure bone mineral of bovine origin manufactured by a unique 1200°C production process.

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botiss biomaterials GmbH

Hauptstrasse 28
15806 Zossen / Germany
Tel.: +49 33769 / 88 41 985
Fax: +49 33769 / 88 41 986
  1. Giesenhagen et al. J Esthet Restor Dent. 2018, 30(6):480-483.
  2. Nord et al. J Oral Implantol. 2019,  45(6):457-463.