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BONEGRAFT BIOMATERIALS

TURKIYE

BONEGRAFT BIOMATERIALS - TURKIYE
www.bonegraft.com.tr
STAND NO. 118

About Us

p Powerbone - Innovative and Functional Biomaterials Solutions Powerbone R amp;D activities are carried out at Ege University Technology Development Center under ISO-7 Class 10000 . Since 2016, production has been carried out in Manisa under ISO-5, ISO 6 and ISO-7 Class 100,1000,10,000 conditions. In addition to its expert employees, high technology and strong capital; serves its customers in full with international quality, management and product certificates. br br Powerbone Granules and Stick amp; Block 100 Synthetic Contains no tissue of human or animal origin therefore carries no risk of disease transmission. Osteoconductive Act as a scaffold and support bone tissue regeneration. Similar to the mineral found in bone tissue. Powerbone polygonal granules have different particle sizes between 0.25-9 mm. Bioresorbable With its optimized porous structure and chemical composition, Powerbone is suitable for the continuous remodeling cycle of healthy bone. B-TCP resorbs over time and be replaced with bone during the healing process. Safe, Biocompatible and Sterile Powerbone is supplied sterile and CE marked as a Class III Medical Device according to Directive 93 42 EEC.Powerbone is tested using: Pre-clinical studies, Biocompatibility tests in vitro and in vivo . Biomechanical tests, Biodegradation tests, Bioburden and Sterility tests. Radiopaque Could be detected via CT and X-ray. Powerbone Silicate Addivite Granule amp; Stick amp; Block Osteoconductive and Osteoinductive Act as a scaffold and support bone tissue regeneration. Similar to the mineral found in bone tissue. Silicate additivity, provides bioactive characteristic to the graft by increasing the protein adhesion. Bioresorbable With its optimized porous structure and chemical composition, Powerbone is suitable for the continuous remodeling cycle of healthy bone. B-TCP resorbs over time and be replaced with bone during the healing process. Safe, Biocompatible and Sterile Powerbone is supplied sterile and CE marked as a Class III Medical Device according to Directive 93 42 EEC.Powerbone is tested using: Pre-clinical studies, Biocompatibility tests in vitro and in vivo . Biomechanical tests, Biodegradation tests, Bioburden and Sterility tests. Radiopaque Could be detected via CT and X-ray The interconnectivity of porous structure and microporosity assist capillary motion of blood and body fluids, enhanced penetration for osteogenic cells, and ossification of the synthetic matrix. For Macroporosity, Powerbone Granules and Stick amp; Block allows deep invasion of bone cells into the matrix. Powerbone polygonal granules have different particle size between 0,25-7 mm. The irregularly shaped granules promote interlocking and improve mechanical stability. Powerbone Dental Putty Powerbone Bonegraft products are designed to repair bone defects caused by surgery or traumatic damage, increase bone growth in non-load-bearing clinical applications, or support the formation of new bone tissue. It can be mixed with bone marrow, blood and other clinically known bone grafts. These products are used in trauma, orthopedics, spine and maxillofacial surgery. Reasons to select Powerbone Dental Putty; Minimal invasive surgical protocol Easier and faster application Ready to use No mixing required Enhance bone regeneration Powerbone Putty Powerbone Bonegraft products are designed to repair bone defects caused by surgery or traumatic damage, increase bone growth in non-load-bearing clinical applications, or support the formation of new bone tissue. It can be mixed with bone marrow, blood and other clinically known bone grafts. These products are used in trauma, orthopedics, spine and maxillofacial surgery. Reasons to select Powerbone Dental Putty; Minimal invasive surgical protocol Easier and faster application Ready to use No mixing required Enhance bone regeneration Powerbone Dental Gel Powerbone Bonegraft products are designed to repair bone defects caused by surgery or traumatic damage, increase bone growth in non-load-bearing clinical applications, or support the formation of new bone tissue. It can be mixed with bone marrow, blood and other clinically known bone grafts. These products are used in trauma, orthopedics, spine and maxillofacial surgery. Reasons to select Powerbone Dental Putty; Minimal invasive surgical protocol Easier and faster application Ready to use No mixing required Enhance bone regeneration Powerbone Chondro Matrix Bonegraft Chondro Matrix is a high-tech scaffold with a flexible and hydrophilic structure, treated with Sodium hyaluronate, sterile, absorbable matrix sponge-like nonwoven Polyglycolic acid PGA . The cortical plate consists of synthetic composite materials PLGA ?-TCP . Cortical Plate is used for bone fixation in trauma and reconstructive surgical operations. Cortical Plate is bioabsorbable. Cortical Plate does not contain human and animal origin tissue or blood derivatives. Cortical Plate graft is safe for patients undergoing MRI or CT scans and is biocompatible with human tissue. The shelf life of Cortical Plate is 3 years with sterilisation by ethylene oxide. Cortical Plate carries a CE mark and is produced in a a ISO 13485 Quality Certified facility.-. Powerbone Bone Cement Bone Cement based on polymethyl methacrylate PMMA is a widely used biomaterial due to its ease of use in clinical practice and especially the long survival rate proven by dentures. ? Common Indications for Bone Cement: total joint replacement are bone and joint reconstructions, fracture fixation and treatment of osteoporotic vertebral fractures. ? Bone Cement consists of two phases, solid and liquid phase. ? To use the product, two phases are mixed in the mixing bowl for 30 seconds. ? Since the product is offered in three different viscosities, low, standard and high, it can be used in different surgical applications at Spine amp;Ortho. ? Products have paste, hardening, maximum temperature and mechanical strength values ??specified in ISO 5833 standard. Interference Screw Implants are supplied sterile and are CE marked. Class III Medical Device according to 93 42 EC medical device directive. Biocompatibility tests in vitro and in vivo , biodegradation tests, bioburden, and stylerity were applied to the products. Implants are used for temporary fixation of bone. Patellar tendon bone and soft tissue grafts in the anterior Cross ligament and posterior cruciate ligament Reconstructions. Powerbright Bone Scraper The Powerbone Bone Scraper is produced from a non toxic polymer. A stainless steel cutter is used to scrape and collect autogenous bone fragments from the chin or ramus area. Powerbone Bone Scraper is designed for use by a suitable qualified clinician. The Powerbone Bone Scraper is a disposable device used to collect autogenous bone particles for use in guided bone regeneration procedures. The resulting bone fragments provide a high volume due to their curved shape, which significantly reduces the amount of augmentation material required and reduces the invasiveness of the intervention. Powerbone Scrapers offer the possibility of obtaining both cortical and spongy bone. Manual removal mixes bone fragments directly with patient blood and retains cellular components such as osteocytes for optimal bone regeneration. Powerbone Flexible Strip Powerbone flexible strip is a bioresorbable synthetic bone graft that provides great hanling with high elasticity for specific cases including bone defects in the pelvis, extremities, and the posterolateral spine fusion. Powerbone flexible strip is composed of silicate additive ?-TCP and PLA based synthetic polymer. Instructions of Implanting Powerbone Flexible Strip; Powerbone Flexible Strip can be applied directly or combination with bone marrow aspirate blood to the surgical site. Wetting Powerbone Flexible Strip increases flexibility. Place Powerbone Flexible Strip into the surgical site just before the closure of the surgical area once all metallic implants are stable. Powerbone Flexible Strip can be cut to fit into a cage. Powerbright Plus 35 hp Powerbright Plus is a tooth whitening agent for office use, belonging to the group of oral care products in the cosmetic product classification and intended for use in the oral cavity. The whitening process is briefly; It is defined as the application of a chemical tooth whitening to the teeth by oxidation and coloring of organic pigments deep in the enamel and dentin tissue to lighten the tooth color. It can only be sold to dentists. Contents. 4X0.5 gr teeth whitening materials 2X1 gr gingival barrier 2 connectors 2 syringe tips Buccal retractor Hydrogen, Peroxide, Glycerol, Sodium Hydroxide,Potassium nitrate, Carbomer Powerbright Plus is a dental agent for:For office use Powerbone Dental Barrier Membrane Specifically engineered for periodontal restorative surgeries and assists in the regeneration of bone and periodontal support tissues. Fabricated from a biocompatible and bioresorbable medical grade poly lactic acid based synthetic polymer with a long history of safe medical use. The Powerbone Barrier Membrane maintains its architecture and completely resorbed 15-20 weeks after implantation. Advantages of Powerbone Dental Barrier Membrane; Prevents fibrous tissue growth in bone zone No risks of virus or disease transmission No requirement for removing membranes due to complete bioresorbtion. Application of Powerbone Dental Barrier Membrane Exterior side of Powerbone Dental Barrier Membrane compose of non-porous poly lactic acid PLA based film to prevent epithelial cells and fibroblast migration. Interior side of Powerbone Dental Barrier Membrane composes of porous poly lactic acid PLA based microfibers to enhance mesenchymal stem cells adhesion, proliferation and differentiation. Three-layer construction of Powerbone Dental Barrier Membrane was constructed to provide healthy regeneration of bone and periodontal support tissues. p

Products:

Bonegraft, Allogreft, Bone Flex, Bone Putty