maxgraft® granules

Processed allograft

For experienced oral and maxillofacial surgeons, allograft bone is  the only real alternative to harvesting the patient’s own autologous bone. This helps preventing well known risks such as donor-site morbidity, infection, post-operative pain, and bone-stability loss. The excellent biological regeneration capability of maxgraft® results in a predictable clinical outcome.

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Rehydration

The processing of maxgraft® products preserves the natural collagen content of the bone tissue and a residual moisture of ~5%. Thus, the products don‘t have to be re-hydrated but are ready for instant use. Nevertheless, rehydration in blood from the defect site or saline solution can facilitate handling and application of granules since the wetted maxgraft® granules stick together. Be aware that hyper-hydration can result in the loss of structural integrity!

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Particle application

Avoid compressing the particles excessively during application; less packed particles leave more space for blood vessel ingrowth and formation of new bone matrix.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with autologous bone

Mixing of maxgraft® granules with autologous bone adds a biological activity (osteoinductive and osteogenetic properties of autologous bone) and supports faster regeneration and formation of new bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Mixing with cerabone®

Mixing of maxgraft® granules with xenogenic materials (cerabone®) combines the advantages of both materials; the biological potential of maxgraft® and the long-term volume stability of cerabone® lead to fast regeneration of strong vital bone.

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

Re-entry

Depending on the defect size, the graft will be incorporated stable within 3-4 months (usage of maxgraft® granules in socket preservation, smaller bone defects, periodontal defects).

[1] Tilaveridis I. et al, The use of mineralized bone allograft (C+TBA) as a single grafting material in maxillary sinus lifting with severely atrophied alveolar ridge (1–3mm) and immediately inserted dental implants. A 3- up to 8-year retrospective study, 2018 Oral and Maxillofacial Surgery, Sep;22(3):267-273.
[2] Simonpieri A. et al. Four-year post-loading results of full-arch rehabilitation with immediate placement and immediate loading implants: A retrospective controlled study. Quintessence Int. 2017;48(4):315-324.
C+TBA Allografts: Presenting the Allotec® process
C+TBA Allografts: Presenting the Allotec® process

maxgraft® blocks

Processed allograft

For experienced oral and maxillofacial surgeons, allograft bone blocks for block augmentation are the only real alternative to harvesting the patient’s own autologous bone. This helps preventing well known risks such as donor-site morbidity, infection, post-operative pain, and bone-stability loss. The excellent biological regeneration capability of maxgraft® results in a predictable clinical outcome.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Contact to local bone

Avoid larger gaps between graft and defect, because a close contact between transplant and local bone ensures block incorporation and faster regeneration.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Rehydration

The production process of maxgraft® blocks preserves the natural collagen and maintains a residual moisture of <5%. Therefore rehydration is not necessary. The product is ready for immediate use.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Combination with cerabone® oder maxresorb®

Additional void volume should be filled with particulate grafting material (e.g. cerabone® or maxresorb®) to improve the esthetic outcome and to protect the soft tissue.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Healing time

The average healing period is about 4 months for smaller defects and 6 months for larger defects.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Avoiding soft tissue perforation

Use flat-headed screws for fixation and avoid sharp edges that might cause a perforation of the overlying soft tissue.

Block augmentation with maxgraft® block and mucoderm® - Dr. K. Chmielewski

Initial situation before surgery. Patient lost central incisors 1 month ago due to endodontic failures

Reconstruction of maxillary ridge with maxgraft® block -Amit Patel

Initial situation with severe maxillary atrophy

Block augmentation with maxgraft® in the maxilla - PD Dr. Dr. F. Kloss

Initial situation - bone defect in maxilla after loosing right canine

Block augmentation with maxgraft® in the maxilla - Dr. R. Cutts

Initial situation: 40 year old female patient with extensive scar tissue after several surgeries restored with a Rochette bridge

Please Contact us for Literature.

Live surgery maxgraft® bone block augumentation -Dr. Haqan
Live surgery maxgraft® bone block augumentation -Dr. Haqan
Fixation maxgraft® block
Fixation maxgraft® block

Jason® membrane

Native pericardium membrane for GBR/GTR

Due to the unique production process, the superior properties of the native pericardium are preserved during the extensive cleaning procedure that is applied for the production of Jason® membrane. Therefore, Jason® membrane shows a natural honeycomb-like, multilayered collagen structure with an increased content of collagen type III leading to a remarkable tear resistance to and a slow degradation of Jason® membrane. This ensures a natural long barrier function, making the Jason® membrane our recommended choice particularly for large augmentative procedures.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Rehydration

The Jason® membrane can be applied dry or pre-hydrated in sterile saline solution or blood from the defect. The initial placement of the dry membrane with subsequent application of the graft material is particularly advantageous for lateral augmentations. After rehydration the membrane can be folded over the defect.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Fixation

Jason® membrane exhibits a remarkable multi-directional tear resistance. Therefore, it can easily be pinned, sutured or even screwed without rupturing.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Exposure

Exposure of Jason® membrane should be avoided, since fast bacterial resorption significantly reduces the barrier function of the thin Jason® membrane. In case of an unstable soft tissue situation or if you expect a wound dehiscence to occur, it is recommended to cover the membrane with a Jason® fleece (where applicable, soaked in antibiotics) to protect the healing area. In case of a dehiscence the wound usually heals without complications by formation of free granulation tissue.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Shaping

Jason® membrane can be cut to the desired shape and size with a pair of scissors - while maintaining sterility. It may be helpful to use appropriate templates for defining the required size of the membrane.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

Placement

Jason® membrane has one rough and one slightly smoother surface. The smoother, fine structured side is marked „G“ at the top right corner and should be placed towards the gingiva. The rougher side should face the bone. However, there is no problem if the membrane is placed the other way around, since the long-term barrier function of the membrane will still provide sufficient protection for the regeneration site.

botiss cerabone® & Jason® membrane for GBR - Clinical case by Prof. Dr. Dr. D. Rothamel

Instable bridge situation with abscess formation at tooth #15 after apicoectomy

botiss cerabone® & Jason® membrane for GBR - Clinical case by Dr. S. Kovalevsky

Implant insertion in atrophic alveolar ridge

botiss cerabone® & Jason® membrane for GBR - clinical case by Dr. S. Stavar

Initial clinical situation with broken bridge abutment in regio 12 and tooth 21 not worth preserving

Advanced vertical augmentation in posterior maxilla with maxgraft® bonering - Dr. A. Isser

Initial situation 57-year old female patient. X-ray scan reveals severe bone loss due to inflammation in region 13. Treatment plan was extraction of teeth 13 and 14 and augmentation after healing.

Augmentation of an atrophic maxilla with maxgraft® bonebuilder - Dr. Dr. Dr. Blume

Pre-operative clinical situation - severe atrophy of the maxillary bone

Please Contact us for Literature.

Immediate implantation and augmentation by Dr. Derk Siebers
Immediate implantation and augmentation by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral sinus lift with maxresorb®
Lateral sinus lift with maxresorb®
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral augmentation on pig jaw by PD Dr. Dr. D. Rothamel
Lateral augmentation on pig jaw by PD Dr. Dr. D. Rothamel
GBR with cerabone® and Jason® membrane – Dr. Alfonso Caiazzo (Italy)
GBR with cerabone® and Jason® membrane – Dr. Alfonso Caiazzo (Italy)
Ridge preservation by Dr. Derk Siebers
Ridge preservation by Dr. Derk Siebers
Augmentation of dehiscence defect by Dr. Marius Steigmann
Augmentation of dehiscence defect by Dr. Marius Steigmann
Lateral one-stage sinus lift with cerabone® and Jason® membrane – Dr. Massimo Frosecchi (Italy)
Lateral one-stage sinus lift with cerabone® and Jason® membrane – Dr. Massimo Frosecchi (Italy)

cerabone®

Natural bovine bone grafting material

The pronounced hydrophilicity of the cerabone® surface supports a fast uptake of blood or saline, thus improving handling. Likewise, its three-dimensional porous network enables a fast penetration and adsorption of blood and serum proteins and serves as a reservoir for proteins and growth factors.The unique manufacturing process based on high-temperature heating removes all organic and potentially antigenic components, making the material safe and free of proteins. cerabone® is a natural bovine bone grafting material that is the preferred material for a high number of dentists.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Rehydration

Rehydration in blood from the defect site or saline solution is not necessary but facilitates handling and application since the wetted cerabone® granules stick together.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Particle compression

Avoid compressing the particles excessively during application; less packed particles leave space for blood vessel ingrowth and formation of new bone matrix.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Healing time

A healing time of at least 6 months is recommended before re-entry to ensure stable integration of the particles.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

Mixing of material

Mixing of cerabone® with autologous bone bring about a biological activity (osteo-inductive and osteo-genetic properties of autologous bone) and supports faster regeneration and improved formation of new bone.

GBR and soft tissue augmentation with cerabone® and mucoderm® - H. Maghaireh & V. Ivancheva

Initial situation: missing teeth #11 & 12 and badly broken #21 root

Intrabony defect treated using collprotect® membrane & cerabone® (1) - Cosgarea & Sculean

Pre-surgical probing reveals a deep intrabony defect on the distal aspect of the upper canine.

botiss cerabone® & Jason® membrane for block augmentation with autologous bone blocks - clinical case by Dr. S. Stavar

Initial clinical situation with single tooth gap in regio 21

botiss cerabone® & Jason® fleece for immediate implantation - Clinical case by Dr. D. Jelušić

Clinical situation before extraction and implantation

Sinus Floor Elevation with maxgraft® bonering and subcrestal implantation in an eggshell thin sinus - Dr. K. Chmielewski

Initial situation: X-ray scan reveals eggshell thin sinus floor (1-3 mm) on both sites of the maxilla; green areas indicate the planned maxgraft® bonerings and red areas the planned implants

Ridge augmentation with maxgraft® bonebuilder and sinus floor elevation – Dr. K.P. Schiechl

Initial clinical situation: Bone defect in the upper right maxilla (teeth #14-16)

Horizontal ridge augmentation with maxgraft® cortico - M.Sc. E. Kapogianni

OPG of the initial situation – provision of missing denture in regio 44 to 47 by a resin-retained bridge

GBR with cerabone® and Jason® membrane in the front tooth region - Dr. H. Maghaireh

Initial clinical situation with gum recession and labial bone loss eight weeks following tooth extraction

botiss cerabone® & Jason® membrane for horizontal augmentation - Clinical case by Dr. M. Steigmann

Three implants placed in a narrow posterior mandible

botiss cerabone® & collprotect® membrane for GBR - Clinical case by Dr. V. Kalenchuk

Clinical situation with narrow alveolar ridge in the lower jaw

botiss cerabone® & Jason® membrane for GBR - clinical case by Dr. S. Stavar

Initial clinical situation with broken bridge abutment in regio 12 and tooth 21 not worth preserving

Restoration of all four incisors with two maxgraft® bonering - Dr. B Giesenhagen

Initial situation pre-op: Central incisors with mobility 3

Advanced vertical augmentation in posterior maxilla with maxgraft® bonering - Dr. A. Isser

Initial situation 57-year old female patient. X-ray scan reveals severe bone loss due to inflammation in region 13. Treatment plan was extraction of teeth 13 and 14 and augmentation after healing.

Immediate implant placement using cerabone® and Jason® fleece - Dr. D. Jelušić

Pre-operative situation showing tooth 21 with deep periodontal pocket. Tooth presented with mobility grade III.

botiss cerabone® & Jason® membrane for GBR - Clinical case by Prof. Dr. Dr. D. Rothamel

Instable bridge situation with abscess formation at tooth #15 after apicoectomy

botiss cerabone® & Jason® membrane for GBR - Clinical case by Dr. S. Kovalevsky

Implant insertion in atrophic alveolar ridge

Block augmentation with maxgraft® in the maxilla - Dr. R. Cutts

Initial situation: 40 year old female patient with extensive scar tissue after several surgeries restored with a Rochette bridge

Socket preservation with cerabone® - Dr. P. Kämmerer

Extraction socket grafted with cerabone.

Socket preservation using cerbaone® and permamem® - Dr. A. Caiazzo

Grafting of the extraction socket with small cerabone® granules.

GBR with Jason membrane® and cerabone® - D. Fontana

Lateral view of the defect in the posterior right maxilla.

[1] Seidel und Dingeldein. Materialwissenschaft und Werkstofftechnik 2004; Vol. 35 No. 4, pp. 208–212
[2] Becker, Organikum, Ambrosius Verlag 1993; Leipzig
[3] Morrison, Boyd, VCH 1986
[4] Murugan et al. Bulletin of Materials Science 2003;26(5):523-528
[5] Tadic, D. and Epple, M. Biomaterials 2004; Vol. 25 No. 6, pp. 987–994
[6] Brown et al. Proceedings of the National Academy of Sciences of the United States of America 2000; Vol. 97 No. 7, pp. 3418–3421
Immediate implantation and augmentation by Dr. Derk Siebers
Immediate implantation and augmentation by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Immediate implantation by Dr. Derk Siebers
Immediate implantation by Dr. Derk Siebers
Lateral one-stage sinus lift with cerabone® and Jason® membrane – Dr. Massimo Frosecchi (Italy)
Lateral one-stage sinus lift with cerabone® and Jason® membrane – Dr. Massimo Frosecchi (Italy)
Lateral sinus lift one-stage by Dr. Derk Siebers
Lateral sinus lift one-stage by Dr. Derk Siebers
Socket seal on pig jaw by PD Dr. Dr. D. Rothamel
Socket seal on pig jaw by PD Dr. Dr. D. Rothamel
Augmentation of dehiscence defect by Dr. Marius Steigmann
Augmentation of dehiscence defect by Dr. Marius Steigmann
Ridge preservation by Dr. Derk Siebers
Ridge preservation by Dr. Derk Siebers
Lateral augmentation on pig jaw by PD Dr. Dr. D. Rothamel
Lateral augmentation on pig jaw by PD Dr. Dr. D. Rothamel
GBR with cerabone® and Jason® membrane – Dr. Alfonso Caiazzo (Italy)
GBR with cerabone® and Jason® membrane – Dr. Alfonso Caiazzo (Italy)