Bonegraft Biyolojik Malzemeler San. VE TIC. A.S. products

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

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.

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 β-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.

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). Bonegraft Chondro Matrix; Contains hyaluronic acid, which effectively supports cartilage formation, Based on PGA and hyaluronic acid and does not contain collagen and animal tissue, Suitable for the regeneration cycle of healthy cartilage, Bioresorbable and support cartilage formation during the healing process, No fragmentation or disintegration during cutting. Interconnective porous structure enables the movement of blood and body fluids to increase penetration for cells.

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&Ortho. Products have paste, hardening, maximum temperature and mechanical strength values specified in ISO 5833 standard.

The ergonomic design of the applicator provides easy removal of the pin and easy fixation of the membrane. The notch, which is about half the length of the pin, allows the pin to attach to the bone. The application of particulate bone regeneration material from the barrier membrane to the local bone, as well as the covering of the augmentation zone by the barrier membrane, can be simplified significantly. Using the one-piece applicator, the titanium pins can be easily taken from the dispenser and applied to the fixation area. No distortion can occur at the working end during machining.

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.