DSI Zenoss Bone Graft is based on a bovine 20/80 cortical-cancellous bone mineral matrix, making it the perfect choice for guided bone regeneration procedures. The unique manufacturing process results in a bone matrix with an interconnecting macro- and microscopic porous structure, supporting the formation and ingrowth of new bone at the implantation site.
DSI Zenoss Bone Graft is an osteoplastic material for the optimization of the bone regeneration process in oral and maxillofacial surgery, as well as in traumatology and orthopedics. It is used as a filler and scaffold to facilitate bone formation and promote wound healing.
The bio-functionality of the DSI Zenoss graft is characterized by its topographic structure, hydrophilic properties, and biological interaction that supports reliable bone formation. This material is designed to fill the missing bone space and encourage new bone tissue growth. Bovine bone is considered a safe and very effective material for bone grafting with dental implants.
DSI Zenoss graft is sterilized by gamma-ray and contains no cellular elements. This eliminates the risk of any disease or unfortunate contamination. It is considered the highest-grade bone substitute in dental bone regeneration â meeting the requirements of clinicians for predictable outcomes.
Granules size is 200-1000Îźm DSI Zenoss has no risk of cross-contamination.
Indications:
Augmentation or reconstructive treatment of the alveolar ridge.
Filling of bony periodontal defects.
Filling of defects after root resection, apicoectomy, and cystectomy.
Filling of extraction sockets to enhance preservation of the alveolar ridge.
Sinus-lifting.
Filling of periodontal defects in conjunction with products intended for Guided
Tissue Regeneration (GTR).
Guided Bone Regeneration (GBR).
Filling of peri-implant defects
Features:
No risk of cross-contamination
Radiopaque
Suited for any surgical bone grafting procedure
Has no antigen-antibody reaction
Biologically active, hypoallergenic
Mimics the natural bone
100% Natural bovine
Fully sterilized and contains no cellular elements
Higher implant survival rates, comparable with implants placed in the native bone
Completely resorbable
Optimal osteointegration - high porosity supports osteoconduction
How to use:
After the necessary preparatory surgical procedures, the granules can be mixed with the patientâs blood or with saline solution in a sterile Dappen dish, before being placed onto the operative site using a dental spatula. 80/20 Saline/Blood proportion is recommended. For large bone defects, Zenoss can be mixed with bone particles from the same patient (autologous bone).
Only gentle compression is advised to allow for optimal revascularization and osseointegration of the bone grafting particles, and the granules should always be covered by a membrane to prevent soft tissue ingrowth into the bone defect.
Re-entry after ridge augmentation or sinus lift procedures with Zenoss Bone Graft should be performed 6 months post-operatively, but this time can be shortened for smaller defects or by mixing with autologous/allogenic bone to improve regeneration and formation of new bone.
