maxgraft® bonebuilder

CUSTOMIZED ALLOGENIC BONE BLOCK

high precision

CAD/CAM TECHNOLOGY

SHORTER TREATMENT TIMES

maxgraft® bonebuilder is a cancellous allogenic bone block made from human donor bone, individually adapted to the patient defect, which is prepared by Cells+Tissuebank Austria in a special purification process (Allotec® process). The three-dimensional fit is planned using state-of-the-art 3D CAD/CAM technology and the block can be inserted with high precision. Surgical time can be significantly shortened and the risk of infection significantly reduced. Increased patient comfort without additional pain and without donor site morbidity is the result1,2.

BLOCK DESIGN WITH CAD/CAM TECHNOLOGY

By planning the ideal fit preoperatively with 3D CAD/CAM technology, optimal contact of the block to the recipient bed can be achieved. Manual adjustment of the cancellous block is usually no longer required. The maxgraft® bonebuilder planning takes place in an interactive exchange between the clinical user and the botiss CAD designers. For more information on customization, please visit the maxgraft® bonebuilder website.

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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® bonebuilder

Art.-No. Content
PMIa Individual planning and production of a bone block max. dimensions 23 x 13 x 13 mm
PMIa 2 maxgraft® bonebuilder, additional block(s) for this patient

bonebuilder dummy

Art.-No. Content
32100 Individual 3D-printed model of the patient’s defect and the planned maxgraft® bonebuilder for demonstration purposes made of plastic

Distribution

With our international network of distribution partners, we are near you in over 100 countries worldwide. In addition to our 360° productportfolio, we offer service, scientific advice and exchange, training and events directly on site from a single source.

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SPECIFIC FACTS

maxgraft® bonebuilder enables complex horizontal and vertical augmentation without burdening the patient by using autologous bone. Due to its high biological regenerative capacity and complete remodeling, maxgraft® bonebuilder represents an alternative to the patient’s own bone block1. The need for a second surgical site is eliminated, surgical time is shortened, and postoperative pain and morbidity for the patient are significantly reduced.

The maxgraft® production process preserves the natural collagen and a residual moisture of <10%. Nevertheless, rehydration is recommended (10 minutes in physiological saline solution). Rehydration can improve the adaptability of the material (especially with large blocks) to the defect.

maxgraft® is processed allograft from human donors. maxgraft® bonebuilder is precisely milled by C+TBA from cancellous bone blocks. The cancellous 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 stringent serological tests in combination with C+TBA’s Allotec® purification process 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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Contact

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Product Management

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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. Kloss et al. Clin Case Rep. 2020, 8, 5.
  2. Jacotti et al. Implant Dent. 2014. 23(1):22-8.
  3. Blume et al.  J Esthet Restor Dent. 2019 31(3):171-178.