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Bonefill ®

Dense, Porous & Mix

Bovine Bone Graft

The highly purified osteoconductive mineral structure is produced from ​natu- ral bone through a multiphase process, complying with the safety ​regulations established by the control agencies. The fresh bone is ​crushed, receiving a se- quence of baths that solubilize the organic ​structures such as, for example, remaining cells, fibers and proteins, ​with only the mineral portion remaining this way in order to avoid the ​induction of possible immunogenic processes in the body. The products ​made of mineralized bovine bone have an expected incorporation of 6 ​to 9 months.

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Surgitime Titanium

Titanium Foil

Titanium Grade I (ASTM F-67) : Thickness 0.04mm.

The fully impermeable Titanium-Foil is ​prestressable, stable and acts as a space maker, ​e.g. for alveolar ridge augmentation. Surgitime ​Titanium SEAL neutral bioelectrically thanks to ​electrochemical passivation and thus contribute ​to an uneventful growth of new bone.

Buccal Proximal

(medial - distal) and Lingual

bone deficiency

Buccal Proximal

(medial - distal)

bone deficiency

Buccal

bone deficiency

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Hydroxyapatite

Synthetic Graft Particulate

Hydroxyapatite, Ca10(PO4)6(OH)2 is a hydrated calcium phosphate, ​major component (about 95%) of the mineral phase of human bones ​and teeth. Used by the body to make up the skeleton due to its ​capacity to act as a calcium and phosphorus reserve. Due to its ​chemical similarity with the chemical phase of bone tissues, it is one of ​the most biocompatible materials known, promoting bone growth in ​regions where it is found (osteoconductive), establishing chemical ​bonds between it and the bone tissue (bioactive), allowing the ​proliferation of fibroblasts, osteoblasts and other bone cells, which are ​not different from the bone surface indicating a high surface chemical ​similarity.

Registro ANVISA 10392710028

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Surgitime Titanium

Titanium Mesh

Surgitime Titanium (Titanium Mesh) is a nonabsorbable titanium screen ​made with pure Titanium (ASTM F-67) and has different sizes, thicknesses ​and hole diameters in order to meet the different clinical needs.

It is supplied sterile, as long as it is kept under ideal storage and preservation ​conditions and the integrity of the pack is not compromised. It is sterilized by ​Gamma Radiation (25kGy).

Registro ANVISA 10392710028

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Bone Graft Kit

Bionnovation Bone Graft Kit composed by a complete line of instruments, are used for the fixation ​and stabilization of bone grafts and membranes (barriers) with the use of screws.

Small and compact, the Bionnovation Graft Kit consists of a practical ​kit that contains all the necessary instruments (drills, drivers and ​screws) for fixation procedures of the bone block and membranes ​(barriers). It is produced with precise tolerances to ensure the easy ​pick-up of screws, stable transfer to the surgical site and rapid ​engagement in the maxilla or mandible. All components of the kit are ​organized and stored together to simplify the procedures.

Registro ANVISA 10392710028

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Bone Grafting Screw

Bionnovation Graft Screw

Bionnovation Graft Screws: Are used for the fixation and stabilization of bone ​grafts and nonabsorbable membranes (barriers) used in guided bone ​regeneration (GBR).

The bone graft screws are temporary and must only stay within the bone ​reparation period because its purpose is to keep the graft and membrane ​stable for consolidation and bone neoformation.

Registro ANVISA 10392710028

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Surgitime PTFE

Nonabsorbable Membrane (PTFE Porous)

Surgitime PTFE is a nonabsorbable membrane composed of Polytetrafluoroethylene, with thickness of 0.10 or 0.25 mm. ​Surgitime PTFE is 100% biocompatible, synthetic and not of animal origin. It is indicated for in orthopedic, neural, ​maxillofacial procedures and other medical or dental surgery procedures.

The polytetrafluoroethylene (PTFE) membranes or mechanical barriers for RTG (Guided Tissue Regeneration) has the ​aim of preventing the migration of epithelial and connective tissue cells, which would cause the inhibition of bone ​growth, promoting suitable space for the formation of a natural fibrin framework, the bone tissue precursor.

The membrane avoids the tissue competition between the connective tissue and the bone, and has the purpose of ​isolating the bone grafts promoting tissue regeneration.

Surgitime PTFE has selective permeability through its porosity, which enables the nutrition of the fibrin framework and ​simultaneously preventing the passage of bacteria.

Registro ANVISA 10392710028