Below are some of the most popular products on DDSGadget.com

Featured Products

Brand

bioGRAF Allograft Particulates are a blend of cortical and cancellous particles, offering the structural strength required to maintain space and volume during the remodeling phase. Used alone or as a composite graft, bioGRAF Particulates are an effective alternative to intraoral graft harvesting. The cortical component provides structural integrity and space-maintaining capability. The cancellous component’s porous architecture promotes osteoconduction and rapid revascularization.

<ul><li>Provides scaffold for cell ingrowth</li><li>Remodels completely</li><li>Predictable guided bone regeneration</li><li>Stabilizes implants after 4-6 months</li><li>Fills voids and extensive bone defects</li><li>Regeneration of periodontal defects</li></ul><h3 class="font-medium leading-tight text-3xl mt-0 mb-2 text-blue-600">bioGraf: Natural Allograft Bone</h3>bioGRAF Allograft Particulates preserve natural collagen and minerals with the bony structure of allograft. The existence of these natural minerals and collagen facilitate remodeling of the host bone suitable for implantation. bioGRAF products are processed to promote new bone formation.<h3 class="font-medium leading-tight text-3xl mt-0 mb-2 text-blue-600">bioGraf: Safe and Effective</h3>The complete line of bioGRAF products has been processed and sterilized to the highest standards set forth by the American Association of Tissue Banks (AATB&reg;) and the U.S. Food and Drug Administration (FDA) regulations. bioGRAF allograft is obtained and processed in conjunction with AATB accredited tissue banks.<h3 class="font-medium leading-tight text-3xl mt-0 mb-2 text-blue-600">bioGraf: Tissue Processing</h3>Tissues are processed in accordance with AATB standards and FDA regulations, as well as additional stringent processes, policies and procedures. Operating to these standards allows you to be provided with one of the purest, most predictable and most proven allografts available today.<img src="https://imagedelivery.net/2w6HjuyuMl15_tznzgwT6g/4f9ff060-2603-47b4-6558-bc980b5f8e00/public" alt="biograf process" class="fr-fic fr-dii">

bioGRAF Mineralized Natural Blend Allograft Cortical/Cancellous, 250-1000 microns

Kerator Overdenture Attachments for Megagen implants.
Each KERATOR Attachment Kit for the Megagen Implant System, comes with:
<ul>
<li>An abutment with carrier, and</li>
<li>A complete Malae Processing Kit (Metal Housing, White Spacer,  and 3 Retention Caps).</li>
</ul>
Please select select your Megagen Implant type below, then select your tissue cuff height.

<h2>Kerator Main Benefits</h2>The KERATOR&reg; Overdenture Attachment System works in the same way as competing systems, but at a fraction of the price.<ul><li>The lowest vertical height in the world.</li><li>Dual Retention (Outside and inside retention) ensures the longest lasting performance</li><li>Easy Insertion and Accurate alignment using self locating design.</li><li>Resilient KERATOR attachment with the superior mobility.</li><li>Plastic carrier for the abutment makes it easier, and safer to handle and check alignment in the mouse.</li></ul>Kerator Male Cap Set<img src="{{media%20url=" alt="" class="fr-fic fr-dii">Colors of the cap determine retention power<iframe src="https://www.youtube.com/embed/rnvmcB3Vcio?rel=0" width="560" height="315"></iframe>About Megagen Implants With its patented innovative knife thread design, the Megagen AnyRidge Implant System delivers superior surgical performance, more primary stability, the ability to load immediately and better aesthetic outcomes, even in the most challenging applications.

Kerator Overdenture Attachment Kit for Megagen AnyRidge Implants

Our New Premium Horizontal PRF Horizon 6 Flex Centrifuge package, provides you with the latest cutting-edge technology for the PRF protocol. Recent research by Miron et al. and Lourenço ES et al. suggests that horizontal centrifugation for Platelet-rich fibrin (PRF) provides benefits over the classical fixed-angle centrifugation. 1,2. The Horizontal Centrifuge provided comes with 2 presets to match specifications needed to create the PRF plugs/membranes (A-PRF), or injectable PRF liquid (iPRF).
Our Premium Horizontal Centrifuge package for PRF includes:
<ul>
<li>1 Horizon 6 Flex Premium Horizontal Centrifuge (see full details below)</li>
<li>1 FREE Pack of 100 Glass Tubes (for A-PRF/Solid PRF)</li>
<li>1 FREE Pack of 50 Greiner Vacuette Plastic Tubes (for iPRF/Liquid PRF)</li>
<li> 1 FREE Pack of 50 Greiner SAFETY Blood Collection Set 21G x 3/4" tubing length 12" (30 cm)</li>
<li>2 Preset Cycles for A-PRF (Solid PRF) and iPRF (Injectable/Liquid PRF)</li>
<li>Optional PRF Instrument &amp; Box Upgrade ($620 Extra)</li>
<li>Designed, built, and supported in the USA</li>
<li>Warranty: 2 years on Centrifuge (lifetime on centrifuge rotor)</li>
</ul>

Dr. Toorani

Excellent machine

The video below is a case showing the use the Horizontal PRF Centrifuge to prepare A-PRF and iPRF (liquid PRF) for Extraction, Implant Removal and Grafting

Horizontal PRF Centrifuge Case

The video below shows the use of the our Horizon 6 Flex Horizontal Centrifuge to produce both Liquid PRF and Solid PRF. The liquid PRF is then used to create a sticky collagen plug with our Bioplug Collagen Plugs. [3,4](Please note: Horizontal centrifugation is a swing-out mechanism process. This means that tubes are always at an angle at rest. However, when spinning starts, they swing out and spin at a horizontal angle out from the axis of rotation, and spin horizontally. This is as opposed to fixed angle centrifugation, where the tubes are always fixed at angle, even when spinning.)

Horizontal PRF Centrifuge Video

The short video below provides highlights from our recent PRF Course given by Dr. Brian Toorani. In the course, Dr. Toorani reviewed phlebotomy techniques and demonstrated centrifugation with both the classic fixed angle Choukroun protocols, and the newer horizontal centrifugation methods, using the DDSGadget <a href="">Horizontal Centrifuge</a>

PRF Course Video

<img style="float: right;" src="https://shop24.ddsgadget.com/media/wysiwyg/horizontal-flex-plus-settings-600.jpg" alt="" />The HORIZON 6 Flex routine centrifuge is completely customizable. The fully digital display makes it easy to set cycle parameters on the fly, including variable run time, speed control, and deceleration. Lid lights flash at the end of each cycle and visually indicate the centrifuge’s status (off when ready, on when running, and flashing when done) from across the room, no matter the noise level. Spin 75-100 mm (3-10 mL) tubes right out of the box. HORIZON 6 Flex arrives ready-to-run without the purchase of any additional accessories.
<h3>Horizon 6 Flex Horizontal Key Features and Benefits</h3>
<ul>
<li>Easy to Use Use the simple, two-button interface to select a preset, or program and record your validated settings on the included label.</li>
<li>Easy to Monitor with LED Lighting Process samples more efficiently. HORIZON's LED lid lighting is off when the centrifuge is ready to load, on when running, and flashing at the end of each cycle.</li>
<li>Engineered for Safety Protect your office with imbalance detection and a shatterproof lid which can only be opened when the centrifuge's rotor is stopped, even if the unit loses power.</li>
<li>Capacity – Up to six (6) tubes Tube Sizes – 3 mL to 10 mL: up to 17 mm x 75 – 100 mm</li>
<li>Fully Programmable – Save and recall 10 easily customizable cycle settings, or choose from 2 presets for PRF</li>
<li>2-Stage Horizontal Rotor – Drucker Diagnostics’ patented swing-out horizontal rotor design produces ideal horizontally separated samples</li>
<li>Cool Operation – Unique design of the convection based cooling system protects the samples even under the heaviest workloads</li>
<li>Automatic Lid Lock – Centrifuge will not run with the lid open and the lid cannot be opened while samples are spinning</li>
<li>Clear Shatter Proof Lid – Allows for safe sample observation and optical calibrations</li>
<li>Reinforced Guard Bowl – Provides maximum safety and durability</li>
<li>Brushless DC Motor – Years of operation with no routine maintenance</li>
<li>Quiet Operation – Enjoy a sound level of just 64 dBA</li>
</ul>
Horizon 6 Flex Horizontal Key Specifications
<ul>
<li>Capacity: 6 x 75-100 mm (3-10 mL)</li>
<li>Max RCF: 2,000 xg</li>
<li>Max RPM: 3,800 RPM</li>
<li>Weight: 12 lbs (5.4 kg)</li>
<li>Dimensions: 9 h x 14 d x 12 w in (23 x 36 x 30 cm)</li>
<li>Warranty: 2 years (lifetime on rotor)</li>
<li>Sound Level – 64 dBA </li>
<li>Voltage – 95 to 253 VAC</li>
<li>Frequency – 50/60 Hz </li>
<li>Max. Power Requirements – 220 Watts</li>
<li>Centrifuge Motor – 1/2 H.P. Brushless DC</li>
</ul>
<h3>Optional PRF Case, PRF Instrument, and PRF Box Upgrade ($585 Extra)</h3>
Our Platinum Horizontal PRF Package includes a full set of PRF Instruments, the PRF Box and a Metal Case.
Full set of 7 instruments that are essential for the PRF technique.
<div style="display: block; margin-bottom: 95px;">
PRF Metal Case 
New! PRF Metal case to hold all you PRF supplies.
 
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/prf-box.jpg" alt="" />PRF Box 
The PRF Box is an extremely important instrument. It helps to: Deliver high quality membranes and constant thickness, and Recover the exudate: hydration of biomaterials.
Preserve the membranes during surgery.
</div>
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/prf-tube-holder.jpg" alt="" />Tube Holder
Is used to hold the tubes and let them rest after the blood drawing.
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_MINI_TRAY.jpg" alt="" />PRF Mini Tray
Used to prepare membranes, Separate the fibrin clot from the red blood cells - Cut the membranes - Fold the membranes - Make «punches»
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_BOWL.jpg" alt="" />PRF Bowl
Is used to mix the membranes cut into small pieces with biomaterials. It can also be used for the cutting: Put the membrane into the bowl and cut it with PRF scissors.
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_SCISSOR.jpg" alt="" />PRF Scissors
Allows to separate easily the fibrin clot from the red cells and to cut membranes into small pieces.
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_TWEEZER.jpg" alt="" />PRF Forceps
Is used to remove and manipulate membranes.
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_TWEEZER_GIRAFFE.jpg" alt="" />PRF Forceps “Giraffe”
The forceps giraffe is intended to tunneling the PRF membranes for surgical soft tissues procedures: introduce the forceps in the tunnel, open the forceps, block the PRF membranes and pull to place the membranes in the correct position.
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_DS.jpg" alt="" />PRF Double Spoon
Allows collecting and handling the bone filling materials in the recipient sites (alveoli, sinus, and goshawks implants).
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_CB.jpg" alt="" />PRF Compactor Big
Allows compacting and tamping the bone filling materials in the recipient sites (alveoli, sinus, and goshawks implants).
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_CS.jpg" alt="" />PRF Compactor Small
Allows compacting and tamping the bone filling materials in the recipient sites (alveoli, sinus, and goshawks implants).
<img style="float: left;" src="https://shop24.ddsgadget.com/media/wysiwyg/344_PAD.jpg" alt="" />PRF Pad
Is used to position the PRF membranes easily, anywhere,using the pad as a cake server. The pointed end of the pad can be introduced in the sinus.
 
 
 
Research References
1. J Biomed Mater Res A. 2018 May;106(5):1373-1380 <a href="https://www.ncbi.nlm.nih.gov/pubmed/29345045" target="_blank" rel="noopener">The in vitro release of cytokines and growth factors from fibrin membranes produced through horizontal centrifugation.</a> Lourenço ES et al.
<blockquote>"The present results demonstrate that blood-derived fibrin membranes with high structural stability and cell content can be generated by horizontal centrifugation, being able of a prolonged production/release of growth factors and pro- and anti-inflammatory cytokines."</blockquote>
2. J Biomed Mater Res A. 2019 Oct;107(10):2257-2271. <a href="https://www.ncbi.nlm.nih.gov/pubmed/31148358" target="_blank" rel="noopener">A novel method for evaluating and quantifying cell types in platelet rich fibrin and an introduction to horizontal centrifugation.</a> Miron RJ et al.
<blockquote>"Horizontal centrifugation produced a significant increase in both the number and concentration of platelets and leukocytes (up to 3.5× higher for either solid/liquid PRF), when compared to either fixed or angled centrifuge."</blockquote>
3. J Contemp Dent Pract. 2019 Nov 1;20(11):1323-1328. <a href="https://www.ncbi.nlm.nih.gov/pubmed/31892686" target="_blank" rel="noopener">Efficacy of PRF vs PRF + Biodegradable Collagen Plug in Post-extraction Preservation of Socket.</a> Ahmed N et al.
4. Implant Dent. 2019 Jun;28(3):220-225. <a href="https://www.ncbi.nlm.nih.gov/pubmed/31124818" target="_blank" rel="noopener">Evaluation of New Bone Formation in Sinus Floor Augmentation With Injectable Platelet-Rich Fibrin-Soaked Collagen Plug: A Pilot Study.</a> Gülşen U et al.

PRF Premium Horizontal Centrifuge Package

Raptos graft is a mixture of allograft mineralized cortical and cancellous chips in a convenient syringe with a filter cap! Curved syringe for better access to site. The cancellous and cortical blend forms an osteoconductive scaffold providing volume enhancement and effective site development for successful dental implant placement.

Video to show how to unbox and prepare the Raptos Syringe for delivery of the graft.

Video Using Raptos

Short video showing showing how you use the Raptos Graft Syringe.

Video How to Use the Raptos Syringe

<h3>Raptos syringe instructions</h3><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/raptos-ins-1.jpeg" alt="" class="fr-fic fr-dii"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/raptos-ins-2.jpeg" alt="" class="fr-fic fr-dii"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/raptos-syringe.jpeg" alt="raptos syringe" class="fr-fir fr-dii"><ul><li>Sourced from premier tissue bank in the US Strict processing procedures are taken by the tissue bank to ensure quality and safe tissue grafts for transplantation. Tissue bank complies with guidelines and regulations with the American Association of Tissue Banks (AATB), Food and Drug and Administration (FDA) and many other state health department regulations.</li><li>Rigorous donor screening Extensive tests for infectious diseases such as AIDS, Hepatitis B&amp;C and Syphilis are performed on all donors recovered by the tissue bank. Each donor is thoroughly evaluated using medical/social history questions, medical records, blood test and culture results, physical examinations and autopsy reports (when performed). The tissue bank&rsquo;s medical director reviews all donor information, and if found acceptable the tissue is released for processing.</li><li>Low dose gamma irradiation Musculoskeletal allografts are processed and sterilized using gamma irradiation following ISO 11137 methodology to provide a sterility assurance level of 10-6.</li><li>Treated with patented cleaning treatment As part of a validated process, cleaning and disinfecting solutions such as alcohol, antibiotics and hydrogen peroxide, along with centrifuges, ultrasonic baths and pressure washes are used during a patented cleaning treatment, to remove viruses, bacteria and cellular material.</li></ul>

RAPTOS Prefilled Syringe: Mineralized Cortico-Cancellous Bone Graft

This graft is a mixture of mineralized, freeze-dried, cortical and cancellous bone chips (250-1000 microns). DALI &trade; , from DDSGadget, is processed by Surgenex, a leading biologics manufacturer that uses its patented Excellion &reg; process to produce the highest quality allograft tissues . The cortical component provides structural integrity and space-maintaining capability. The cancellous component’s porous architecture promotes osteoconduction and rapid revascularization.

Description These allografts are used in situations where a human allograft is appropriate, such as dental bone grafting procedures. The allograft particulates are, low-dose, gamma-irradiated particles of allogeneic human bone. Tissue Source: Surgenex Surgenex&reg; is an industry leading biopharmaceutical company, providing regenerative medicine solutions that set the industry standard in quality and safety. Surgenex&reg; uses its patented Excellion&reg; process to produce minimally manipulated products that adhere to strict regulatory standards. Following these standards allows Surgenex&reg; to sell approved allograft products with confidence to healthcare providers. This human tissue allograft is processed and packaged by Surgenex. All tissue was recovered, processed, stored and distributed for use in accordance with the standards of the American Association of Tissue Banks (AATB), the FDA requirements for Human Cellular and Tissue Based Products (HCT/Ps 21 CFR Part 1271), and applicable State regulations. Surgenex&reg; has determined the Donor to be eligible, based on the results of screening and testing. Screening includes a review of medical and social history, available hospital records, infectious disease testing, autopsy reports (if performed), and physical examination of the Donor, at the time of recovery. The Donor has been tested using FDA licensed, approved, or cleared donor screening test kits. Communicable disease testing has been performed by a laboratory registered with the FDA to perform donor testing in accordance with the Clinical Laboratory Improvement Amendments of 1988 (CLIA) and 42 CFR part 493, or that has met equivalent requirements as determined by the Centers for Medicare and Medicaid Services (CMS).Contraindications The presence of infection at the transplantation site is a contraindication for use of musculoskeletal allografts. The presence of gross infection at the transplantation site is a contraindication for use of skin allografts. Contraindications customary to the use of bone grafts should be observed. In addition, bioGRAF should not be used in patients with: &bull; Osteomyelitis at the surgical site &bull; Metabolic diseases (diabetes, hyperparathyroidism, osteomalacia) &bull; Severe renal dysfunction &bull; Severe liver disease &bull; High-dose therapy with corticosteroids &bull; Vascular impairment at the implant siteWarnings &bull; Discard grafts when mishandled, or when possible contamination of the graft has occurred. &bull; Return to the supplier, any package in which the sterile barrier has been compromised. &bull; Do not re-sterilize. &bull; Unused bone should be properly discarded. &bull; Single patient use only.Precautions: &bull; Federal law (USA) restricts use to licensed cliniciansHandling and Preparation Graft preparation instructions are intended as guidelines as part of established surgical techniques. They are not intended to replace or change standard procedures or institutional protocols.Caution: All preparation should be performed using aseptic technique. STORAGE REQUIREMENTS: &bull; Store at ambient temperature &bull; Do not freeze. No refrigeration is necessary. THIS ALLOGRAFT IS SUPPLIED STERILE This tissue allograft has been sterilized, via Gamma irradiation, to a SAL of 10-6 (Sterility Assurance Level). Allografts are processed using some or all of the following agents: physiological buffers, acids, alcohols, hydrogen peroxide and traces of these may remain. STORAGE Maintain the tissue allograft at ambient room temperature. PREPARATION OF FREEZE-DRIED TISSUES ALL FREEZE-DRIED TISSUE SHOULD BE REHYDRATED FOR A MINIMUM OF 20 MINUTES OR UNTIL SURGEON&rsquo;S DESIRED HANDLING CHARACTERISTICS ARE MET. EXTENDED REHYDRATION TIME (UP TO 1 HOUR) IS RECOMMENDED FOR ANY TISSUE THAT DOES NOT FULLY RECONSTITUTE WITHIN THE INITIAL RECONSTITUTION TIME. 1. Place the graft in a basin with sterile saline (0.9%), Lactated Ringer&rsquo;s, or other sterile isotonic solution for a minimum of 20 minutes. If the supplied allograft is a powdered dental particulate, small amounts of the aforementioned solutions may be added to the jar and mixed with the allograft. 2. Extended rehydration time (up to 1 hour) is recommended for any tissue that does not fully reconstitute within the initial reconstitution time. 3. Allografts must be used within six hours after rehydrating if the allograft is stored at room temperature. The allograft must be stored with proper precautions to prevent contamination

DALI Mineralized Cortical Cancellous Bone Mix, Large Particle, 250-1000 um

The PTFE 4-0 suture with a 16 mm reverse cutting needle, 3/8 circle, is the most popular of the smaller 4-0 sutures, especially for dental implant and bone grafting procedures. Cytoplast Comparison: CS0618RC. 
<ul>
<li>16mm, 3/8 Circle - 18"(45cm)</li>
<li>100% Medical Grade PTFE sutures&nbsp;. Undyed, Uncoated, Monofilament.</li>
<li>Eliminates bacterial wicking,&nbsp;</li>
<li>Biologically inert and chemically non-reactive.</li>
<li>Excellent handling and knot security. Little or no package memory</li>
<li>Sold in Package of 12 sutures. </li>
</ul>

<h2>PTFE Sutures Main Features and Benefits</h2><ul><li>Ultra sharp needle point for atraumatic tissue penetration. Needle is coated with silicone for smooth tissue passage.</li><li>Nonresorbable: Keeps the surgical site reliably closed</li><li>Monofilament Construction: Eliminates bacterial wicking. Thread is Undyed, Uncoated.</li><li>Excellent Soft Tissue Response: PTFE suture&#39;s unique softness and smoothness enables it to go through soft tissues minimizing micro- damage reaction around tissue duct, which prevents from bacterial colonization in deeper layers of the wound.</li><li>Biologically inert and chemically non-reactive: 100% Medical Grade PTFE</li><li>Promotes Wound Healing: In contrast to braided sutures, especially those made from absorbable materials, PTFE does not absorb blood, saliva, bacteria and food residues. This promotes wound healing.</li><li>Not subject to weakening by tissue enzymes: Despite its soft and delicate nature, PTFE firmly supports tissues during the whole healing process, in contrast to absorbable materials which maintain tissues only in the early stages of healing due to the presence of enzymes in the mouth.</li><li>Little or no package memory: soft handling and knots securely. The thread does not retain the coiled shape after unpacking, which makes it easier to work with.</li><li>Great fluency among tissues</li><li>Comfortable and soft for the patient: not stiff like most monofilaments. The surgical knot made with a PTFE suture is durable and does not loosen. The ends of the suture do not cause irritation of the cheek, lips and tongue, unlike suture materials based on various monofilament fibres, which additionally may contribute to the formation of viral changes on mucous membrane.</li><li>Ultra High tensile strength: does not weaken when moistened. Provides permanent support.</li></ul><h2>PTFE Suture Applications</h2>PTFE sutures thanks to being completely non-absorbable and biologically inert, cause minimal inflammatory response in the moist environment of the oral cavity, that&rsquo;s why they are an excellent choice for any:<ul><li>Bone grafting procedures&nbsp;</li><li>Soft tissue grafting&nbsp;</li><li>Guided tissue regeneration&nbsp;</li><li>Implant surgery&nbsp;</li><li>Periodontal surgery&nbsp;</li><li>Ridge aumentation&nbsp;</li></ul><h2>About PTFE Sutures</h2>The PTFE Suture, is monofilament, synthetic, non-absorbable surgical suture composed of 100% polytetrafluoroethylene without any additives. The suture undyed and uncoated.PTFE is a unique biomaterial in that it is inert and chemically non-reactive. In addition, the monofilament construction prevents bacterial wicking which is associated with braided sutures. Therefore, PTFE sutures are ideal for any implant, periodontal and bone graft surgery where the usage of a monofilament suture with low bacterial adhesion is recommended.

PTFE Suture, 4-0, FS3 (C22), 12PK

The OsteoGen ® Plug combines bone graft with a collagen plug to yield the easiest and most affordable way to clinically deliver bone graft for socket preservation and ridge maintenance without the use of a membrane. Watch video below.
<ul>
<li>Eliminate hassle of mixing particulate grafts. Eliminate graft wash out.</li>
<li>Radiolucent on day of surgery – Radiopaque in 3-6 months </li>
<li>Sold in packs of 5 or packs of 10.</li>
<li>Available in Large: 10mm in Diameter x 20mm in Length</li>
<li>OsteoGen® proven safe, and clinically effective for use with implants for over 30 years.</li>
</ul>

Kevin Mischley DMD

Osteogen Plug is a No Brainer

<h3>OsteoGen Plug Case</h3>
<img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/compress/1616171893324-osteogen-case-1-1.jpg.jpg" alt="OsteoGen Bone Grafting Plug Case" max-width="100%" /> <img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/compress/1616171903125-osteogen-case-1-2.jpg.jpg" alt="Osteogen Case 2" max-width="100%" />
<h3>OsteoGen Plug Key Features and Benefits</h3>
<ul>
<li>Just drop the plug into your extraction site following curettage and debridement to induce a regional acceleratory phenomenon and suture over top.</li>
<li>Combines our OsteoGen ® Bioactive Resorbable Calcium Apatite with a bovine achilles tendon collagen matrix to create a structure that mimics the organic and inorganic components of physiologic bone. </li>
<li>The Bovine Achilles Tendon collagen carries the bone graft for easy and efficient delivery to the site, eliminating the hassle and time spent mixing and packing particulate grafts while also eliminating the potential for graft wash out. </li>
<li>OsteoGen® is a bioactive and resorbable calcium apatite crystal bone graft that is physicochemically &amp; crystallographically similar to human bone. </li>
<li>The Type I collagen acts as a wound dressing not only to stabilize the clot, but also to absorb and deliver blood flow to the slowly resorbing graft, a feature critical for the initiation of bone formation and early angiogenesis. </li>
<li>The collagen found in the OsteoGen® Plug provides a scaffold for keratinized tissue to develop over the grafted site. </li>
<li>Radiolucent on day of surgery – Radiopaque in 3-6 months </li>
<li>Non-Ceramic highly porous crystals physicochemically similar to trabecular bone </li>
<li>OsteoGen® proven safe, reliable and clinically effective for use with implants for over 30 years </li>
<li>Available in Large: 10mm in Diameter x 20mm in Length</li>
</ul>
The OsteoGen® Bone Grafting Plug is the easiest and most affordable way to clinically deliver bone graft for ridge maintenance and socket preservation. The idea is simple - we take a collagen plug and fill it with our OsteoGen® non-ceramic bone graft crystals to create the OsteoGen® Bone Grafting Plug. The result is a bone graft combined with a collagen plug for ease of clinical delivery – all at the introductory special price of only $50 per extraction without the need for a membrane.
The OsteoGen® Bone Grafting Plug combines our OsteoGen® Bioactive Resorbable Calcium Apatite with a bovine achilles tendon collagen matrix to create a structure that mimics the organic and inorganic components of physiologic bone.
OsteoGen® is a bioactive and resorbable calcium apatite based bone graft that is physicochemically and crystallographically similar to human bone.1 The OsteoGen® non-ceramic production process yields a resorbable bone graft with a unique Ca:P ratio that is NOT a ß-TCP and NOT a non-resorbable dense ceramic HA, nor is it a biphasic mixture of the two.

OsteoGen Bone Grafting Plug

Neomem, the standard resorbable collagen membrane, is a Type 1 bovine collagen matrix indicated for use in guided tissue procedures to enhance wound healing. Watch video and review Neomem cases below. 
<ul>
<li>Derived from highly purified type I collagen fibres from bovine Achilles tendon.</li>
<li>Sustained function. Resorption Time: 26 - 38 weeks (6 - 9 months). </li>
<li>Compare to: Cytoplast&reg; RTM*, ACE RCM6 </li>
<li>Maybe sutured or tacked. Suture pullout strength between 290g and 350g.</li>
<li>Cell occlusive - retards epithelium down growth</li>
<li>Macromolecular pore size allows nutrient transfer</li>
<li>Exceptional clinical performance and easy in situ placement. Place wet or dry.</li>
</ul>

docphil

Membrane of choice

<h3>Neomem Additional Information</h3><ul><li><a href="#features">Features and Benefits</a></li><li><a href="#video">Surgical Video</a></li><li><a href="#cases">Clinical Cases</a></li></ul><h3>Neomem Key Features and Benefits</h3><ul><li>Derived from highly purified type I collagen fibres from bovine Achilles tendon.</li><li>Higher mechanical strength for membrane stabilization in situ using either sutures or resorbable tacks. Suture pullout strength between 290g and 350g</li><li>Longer in vivo stability and resorption time, 26 ‑ 38 weeks, for sustained function.</li><li>Optimized flexibility and rigidity for better space maintenance which allows for desired tissue in-growth.</li><li>Either side of the Neomem can be placed towards the soft tissue or bone.</li><li>Easily trimmed and placed, wet or dry.</li><li>Gamma irradiated to sterilise/Nonpyrogenic</li></ul><h3>Neomem Cases</h3><h4>Case 1: Implant Placement with Simultaneous Guided Bone Regeneration Dr. Steven Faigan, Certified Specialist in Periodontics, Kelowna, British Columbia</h4><ul class="products-grid cols-3 first odd"><li class="item first"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-1-a.jpeg" alt="" class="fr-fic fr-dii"> Fig. 1: Resorption of the buccal bone</li><li class="item"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-1-b.jpeg" alt="" class="fr-fic fr-dii"> Fig 2: Grafted atrophic ridge</li><li class="item last"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-1-c.jpeg" alt="" class="fr-fic fr-dii"> Fig 3: Neomem Resorbable collagen membrane</li><li class="item first"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-1-d.jpeg" alt="" class="fr-fic fr-dii"> Fig 4: Regeneration of bone</li><li class="item"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-1-e.jpeg" alt="" class="fr-fic fr-dii"> Fig 5: Final restoration</li><li class="item last">&nbsp;</li></ul>A 63 year old female patient presented requesting implants as a treatment modality to replace several missing posterior teeth in the lower left quadrant. Her natural teeth had been extracted 20 years earlier without replacement, resulting in a significant horizontal ridge deficiency. It was explained to the patient that although implants represented an ideal treatment option, it would be necessary to simultaneously augment the bone to allow for optimum bone integration and stability of the implants. The patient agreed to the proposed surgical and prosthetic treatment plan. Two threaded, cylindrical, external hex Osseotite&reg; implants (3I, Implant Innovations Inc., Palm Beach Gardens, FL) were placed into the areas of #35 and #37. With optimum implant positioning, and given the horizontal resorption of the host bone in the area, approximately 5-6 threads were exposed on the buccal surface of the implant in site #35 and 3-4 threads on the buccal surface of #37 (fig. 1). 1.0 cc of DynaGraft&reg; II Putty (Citagenix Inc. Montreal, Quebec) was used to augment the deficient ridge and cover the exposed threads of the implants. DynaGraft&reg; II is a bioassayed DFDBA offering the inductive capability required to achieve regeneration of vital bone. DynaGraft&reg; II comes supplied pre-mixed in a reverse phase medium allowing for ease of handling and accurate placement of the material. With simple finger manipulation, the material can be molded into the ideal three dimensional shape to augment the deficient area (Fig. 2). Once in position, the viscosity of DynaGraft&reg; II reduces the risk of dislodgement during final placement, irrigation and flap closure. A 30x40mm Neomem&trade; (Citagenix Inc., Montreal, Quebec) GBR resorbable membrane was placed over the graft to assist in bone graft containment and to eliminate connective tissue and epithelial invagination into the surgical site (Fig. 3). Reapproximation of the flaps was achieved and tension free primary closure established utilizing 5-0 chromic gut sutures. A two stage submerged protocol was undertaken given the simultaneous GBR procedure. Healing was uneventful and the implants were uncovered at 9 months. Clinical evaluation confirmed the apparent regeneration of bone on the buccal aspect of the mandible with coverage of the exposed implants threads (Fig. 4). At this time, the implants were stable and integrated and 3i&rsquo;s emergence profile transitional healing abutments were placed. A soft tissue healing period followed for the next 6 weeks. Prefabricated, preparable GingiHue&trade; Post (3i) prosthetic abutments were inserted and the patient restored with a ceramometal cemented fixed bridge (Fig. 5). Without the assistance of augmentation materials, endosseous implants would be limited to only those patients that presented with alveolar ridges with adequate bone volume. The predictability of guided bone regeneration techniques has increased the number of implant candidates and has facilitated prosthetically driven restorations.<h4>Case 2: Autogenous Bone Graft Harvesting for Implant Dehiscence Defect Dr. Doug-Seok Sohn, Associate Professor, Chair Department of Oral and Maxillofacial Surgery Daegu Catholic University Hospital, Daegu, South Korea</h4><ul class="products-grid cols-3 first odd"><li class="item first"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-a.png" alt="" class="fr-fic fr-dii"> Fig. 1: Bridge in place before extractions</li><li class="item"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-b.png" alt="" class="fr-fic fr-dii"> Fig 2: Osteotomies using MIS drill guide</li><li class="item last"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-c.jpeg" alt="" class="fr-fic fr-dii"> Fig 3: Autogenous bone harvesting</li><li class="item first"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-d.jpeg" alt="" class="fr-fic fr-dii"> Fig. 4: RotoGrafter filled with graft</li><li class="item"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-e.jpeg" alt="" class="fr-fic fr-dii"> Fig 5: Dehiscence defects around implants</li><li class="item last"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-f.jpeg" alt="" class="fr-fic fr-dii"> Fig 6: Autogenous graft in place</li><li class="item first"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-g.jpeg" alt="" class="fr-fic fr-dii"> Fig. 7: Neomem Collagen membrane to protect grafted bone</li><li class="item"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-h.jpeg" alt="" class="fr-fic fr-dii"> Fig 8: Tension free primary closure</li><li class="item last"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/neomem-case-2-i.jpeg" alt="" class="fr-fic fr-dii"> Fig 9: Post-op radiograph</li></ul>The patient presented with a fourunit bridge that was supported by the second premolar and third molar, which were both unsalvageable (Fig. 1). The bridge was removed, the two teeth were extracted and the site was allowed to heal for six weeks. In this case, no grafting material was used at the time of extraction.The treatment plan included three endosseous implants to be placed posteriorly to the first premolar to support a fixed prosthesis. At the time of the implant placement surgery, significant horizontal bone loss was observed. Implant sites for three MIS implants were prepared using the MIS drill guide (Fig. 2). Following this and prior to implant placement, an autogenous bone graft was harvested at the implant surgical site using the RotoGrafter&trade;. It was attached to a 16:1 contra-angle handpiece and the drill speed was set to 1000 RPM. The Rotografter was used to perforate the buccal plate inferior as well as distal to the implant sites, thus allowing bone to be collected without compromising implant placement (Fig. 3-5).Upon insertion of the three root form implants, dehiscence defects were noted ranging from 2mm to 5mm buccally and coronally around the implants. The 100% autogenous bone graft collected from the RotoGrafter was placed in the deficient areas (Fig. 6). A resorbable collagen membrane (Neomem, Citagenix Inc.) was used to cover the graft site and a tension free suture technique was employed to achieve primary closure (Fig. 7-8).*Cytoplast&reg; is a registered trademark of Osteogenics Biomedical, Inc.