Augmentation of the alveolar ridge, creating "sticky bone" (combined with PRF), filling periodontal defects, root resection, apicoectomy, and cystectomy
DSI Zenoss Chips is a biocompatible bone mineral matrix made from bovine bone. All the organic components are has been removed according to a controlled and validated multistage purification process. DSI Zenoss Chips is a highly osteoconductive slowly resorbed biomaterial.
DSI Zenoss Chips stabilize the graft, maintaining the volume and the form of augmented sites and increasing the bone density. Such an approach using the DSI Zenoss Chips shows impeccable long-term implant survival results. The inorganic bone matrix of DSI Zenoss Chips has macro- and microscopic structures similar to human bone.
The natural micro-porous consistency plays a critical role in improving the osteoinduction of the scaffold. The macroporous architecture, in turn, allows cell infiltration and body fluid circulation for excellent osseointegration.
âLarge particles -"Chips" of 1000-5000Îźm size DSI Zenoss has no risk of cross-contamination.
Indications:
Augmentation or reconstructive treatment of the alveolar ridge.
Perfect shape for creating "sticky bone" (combined with PRF)
Filling of bone periodontal defects.
Filling of defects after root resection, apicoectomy, and cystectomy.
Filling of extraction sockets to enhance preservation of the alveolar ridge.
Elevation of the maxillary sinus floor.
Filling of periodontal defects in conjunction with products intended for Guided
Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR).
Filling of peri-implant defects in conjunction with products intended for Guided
Bone Regeneration (GBR).
Features:
The unique micro and macroporous structure
Slow resorption
Physically and chemically similar to human bone
Superior stability
Low immunogenicity
Excellent biocompatibility
Highly osteoconductive
Stabilize the graft
Maintaining the volume and the form of augmented sites
Increasing the bone density
How to use:
We suggest mixing DSI Zenoss chips with the patientâs blood or with a physiological saline solution before the implantation. The chips are placed into the defect, using sterile instruments (spatula or spoon). The use of excessive force will result in the crushing of particles and loss of trabecular architecture.
In situ, modeling may be performed with a sterile spatula or other suitable instrument. Overfilling of the defects should be avoided. It is advisable to cover the graft with a membrane barrier When closing the wound, the soft tissue flap should completely cover the implanted graft and should be fixed by sutures.
