
Powerbone – Innovative and Functional Biomaterials Solutions
Powerbone R&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.
- Powerbone Granules and Stick & Block
- Powerbone Silicate Addivute granule & Stick & Block
- Powerbone Putty
- Powerbone Dental Gel
- Powerbone Dental Putty
- Powerbone Dental Barrier Membrane
- Powerbone Flexable Strip
- Powerbone Chondoro Matrix
- Powerbone Bone Cement
- Powerbone Titanyum Pin Set
- Powerbine Interference Screw
- Powerbone Forehead
- Powerbone Transbleph
- Powerbright Plus %35 hp
- Bowerbone Cortical Plate
- Pwerbone Peri-Implant Ring
- Pwerbone PowerBright Bone Scraper
■ %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. ß-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.
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. ß-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 & 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 / 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 / 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 / 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.
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.
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.
Instructıons 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).
The cortical plate consists of synthetic composite materials (PLGA + β-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.-.
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.
FEATURES
Extremely comfortable grip ergonomics for easy use
- Titan pin acquisition
- Functional design
- Safe and easy opening with one hand control
- Suitable for absorbable and non-absorbable.
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.
Optimized Size for Sensitive Applications ForeHead provides a smaller implant scale with the same predictability and safety for finer local precision applications in the forehead area. It also offers a suitable solution for patients with thicker, soft tissue and forehead skin.
An ultra-thin platform with multiple ultra-thin spines that are unaffected by palpability but provide sensitivity for patients with all the physical characteristics of the larger ForeHead scale.
Fast Way to achieve upper periorbital region rejuvenation. This device provides versatility to combine the removal of the upper eyelid skin with the repositioning of the brow and upper eyelid skin in a single surgical session.
Using the required Upper blepharoplasty incision as an entry port, TransBleph assists the surgeon in a holistic approach to the upper periorbital region. The device is easy to implement in the field and no extra hardware is required, meaning fewer tools for installation, handling and maintenance.
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
- •4×0.5 gr teeth whitening materials
- 2×1 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
- The cortical plate consists of synthetic composite materials (PLGA + β-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.
Peri-Implant-Ring material consists of silicate-added ß-TCP embedded inside a PLA based synthetic polymer lattice.
The product is presented as a flexible ring structure.
Powerbone Flexible Ring does not contain human and animal origin tissue or blood
derivatives.
Peri-Implant-Ring is sterilized by Gama radiation and is osteoconductive and osteoinductive.
The shelf life of the product is 3 years.
Peri-Implant Bone Ring Benefits:
- Predictable bone augmentation.
- No need to harvest bone.
- Associated risk of infection donor site morbitidy and pain can be avoided.
- Improved initial implant stability.
- Successful in ridge defects effective in sinus floor elevations.
- Reduces the overall number of procedures and treatment time is reduced for a gratifying patient acceptance.
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.
Start with the customer – find out what they want and give it to them.
Creative and Healthy Solutions
In the modern production facilities of Bonegraft; all electronically controlled; Production area in the cleaning class of ISO7 according to ISO 14644 , Class 10.000 according to Fed.St.209D, ISO5 according to ISO 14644, monitored in real time 7 days and 24 hours for all production parameters such as temperature, humidity, pressure differences, air change rate and so on. According to Fed.St.209D, there are clean rooms for packaging in Class 1000 cleanliness class.,
All raw materials and equipment used in the production processes are procured from companies of European and American origin, which are at the highest level in terms of technology.
Our company has TSE approved TS EN ISO 13485 quality management system certificate.














