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<p>The Amnion Chorion membrane is an ideal barrier membrane for many dental applications. The DALI &trade; amnion chorion membrane, manufactured by Surgenex, is a dehydrated amniotic membrane allograft that is shelf-stable and minimally manipulated to maximize the benefits of the amniotic membrane.</p>
<ul>
<li>Multi-year shelf-life from manufactured date when stored at ambient temperature.</li>
<li>No need to trim or fixate due to unmatched adhesion.</li>
<li>No need to pre-hydrate.</li>
<li>No orientation. Place up or down.</li>
<li>Can be left exposed.</li>
<li>Fully resorbs in 8 to 12 weeks.</li>
<li>Possesses inherent antibacterial properties. [1]</li>
<li>Performs well even when exposed.</li>
<li>Can be used a primary membrane or adjunct.</li>
</ul>

<p>This is an excellent video which goes over the various use cases for amnion-chorion membranes. </p>

video for amnion

<h2>Why Amniotic Membranes?</h2><p>The amniotic membrane is the natural layer surrounding the fetus in the womb. The membrane is essentially composed of two main layers: the amnion &ndash; the layers closest to the fetus, and the chorion &ndash; the layers closest to the mother. Together these layers provide a protective barrier adept at remodeling to accommodate the growing fetus. This protective feature makes amniotic membranes ideal for homologous use as a barrier in a variety of applications. Amniotic membranes have been used for decades in varied fields such as ophthalmology, reconstructive surgery, and burn treatment. The amnion-chorion membrane from Surgenex is a minimally manipulated, dehydrated, non-viable cellular amnion-chorion membrane. The manufacturing process preserves the membrane to maintain its therapeutic properties while preparing it for shelf-stable storage, and flexible use in a variety of treatment applications. The inclusion of the chorion part of the amnion enhances the rigidity of the membrane.</p><h2>Key Benefits of Amnion Chorion Membranes</h2><ul><li><strong>No Trimming Necessary:</strong> Amnion-chorion membranes do not need to be trimmed prior to use in most procedures. After placement, the excess membrane can be folded over itself. The membrane is safe to touch adjacent tooth/root surfaces. If trimming is required, use sharp dry scissors.</li><li><strong>Orientation Does Not Matter:</strong> During placement of amnion-chorion membranes, orientation does not matter. They may be placed up or down.</li><li><strong>Easy Stabilization:</strong> No sutures or tacks are required to stabilize amnion-chorion membranes. The graft may be anchored to the surgical site by the method of choice and rapidly rehydrates once fixed. Basically, amnion-chorion membranes &nbsp;will stick to any hydrated surface, adhering like shrink wrap.</li><li><strong>No Pre-Hydration Necessary:</strong> Place dry and allow it to hydrate to the site. You can also briefly hydrate the membrane prior to placement with drops of sterile saline. Note that excessive bleeding can cause amnion-chorion membranes to slide. Hemostasis should be achieved prior to placement.&nbsp;</li><li><strong>Non-Primary Closure is Acceptable:</strong> Amnion-chorion membranes may be left exposed to the oral environment. When left exposed strict adherence to post-surgical protocols are necessary. [2]</li><li><strong>Minimally Invasive:</strong> No flap elevation required as you can simply tuck an amnion-chorion membrane under the gingival margin.</li></ul><h2>Brief Instrument Guidance for Amnion Chorion Membranes</h2><p>Because amnion-chorion membranes are incredibly adhesive when hydrate, Use dry instruments when the membrane is dry and wetted instruments once membrane is wet/hydrated, as this will prevent the membrane from sticking to the holding instrument. A common technique for placing amnion-chorion membranes is a 2-instrument method: dry instrument (e.g. plier/forcep) to place and anchor, and a wet instrument (e.g. periosteal elevator) to hydrate and tuck the membrane.</p><h2>Amniotic Membranes Procurement, Processing and Safety</h2><p>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.</p><p>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)</p><p>The Surgenex process extracts the membrane from the placental tissue, leaving only the amniotic membrane layer which is then dehydrated into a sheet-like product. The membrane&#39;s minimally manipulated process retains the benefits of the amniotic membrane providing clinicians with a flexible sheet for a variety of treatment applications.</p><p>The amnion membrane is thoroughly tested for safety and efficacy. We pride ourselves on safety standards that exceed regulatory requirements by performing additional serological tests missed by our competitors. SURGENEX&reg; clears allografts using a third-party serological lab, followed by quality inspections on site.</p><p>The amnion family of allografts are processed in compliance with all current Good Tissue Practices as mandated by the United States Food and Drug Administration and the American Association of Tissue Banks. Surgenex prides themselves on quality standards and testing that exceed industry standards.</p><p><img src="https://imagedelivery.net/2w6HjuyuMl15_tznzgwT6g/171806af-a4cd-459f-6e06-df1068dae200/ddsnext" alt="amnion processing safety" class="fr-fic fr-dii"></p><h3>References</h3><p>1. Ashraf H, Font K, Powell C, and Schurr M. <a href="https://pubmed.ncbi.nlm.nih.gov/31379946/" rel="noopener noreferrer" target="_blank">Antimicrobial Activity of an Amnion-Chorion Membrane to Oral Microbes.</a> International Journal of Dentistry, 2019. 2019: p. 7 (Amnion-chorion membrane (ACM) was proven to be as bactericidal as paper discs inoculated with tetracycline at its minimum bactericidal concentration. The ACM bactericidal property may be beneficial in the early wound healing process.)</p><p>2. Clin Adv Periodontics. 2020 Dec 31. doi: 10.1002/cap.10144. <a href="https://pubmed.ncbi.nlm.nih.gov/33382524/" rel="noopener noreferrer" target="_blank">Amnion-Chorion Membrane in Open-Wound Approach for Localized Horizontal Ridge Augmentation: A Case Series</a> Report Shan-Huey Yu et al.</p>

DALI Amnion / Chorion Membrane

<p>CevOss bone is made of deproteinized bovine bone and is indicated in bone regeneration. Thanks to its natural origin, it is chemically and structurally comparable to mineralized cancellous human bone (natural nanocrystalline apatite). The highly purified osteoconductive mineral structure is obtained from natural bovine bone through a manufacturing process that guarantees a 96% phase purity in strict compliance with international standards.</p>

<ul>
<li>Substantially equivalent to BioOss ®<sup>1</sup> and NuOss ®</li>
<li>Sterilized with gamma-radiation at 25kGy. No potential immunological or infectious risks.</li>
<li>Easy handling of material allows for precise graft placement. Adapts to the cavity shape.</li>
<li>The high volume of interconnected pores promotes new bone formation and growth</li>
<li>Porosity of material allows for thorough revascularization</li>
<li>Particle structure helps to maintain space</li>
<li>Available in .25-1mm particle size Particle Size: 0.5CC, 1.0CC and 5.0cc. Choose below.</li>
</ul>


The mineral bone matrix of CevOss has a macro- and micro-porous structure similar to human cancellous bone. Due to the large interconnecting pore volume and the natural composition, the formation and growth of new bone at the implantation site is promoted. Over time, CevOss is partially remodeled by osteoclasts and osteoblasts (physiological remodeling). Due to its properties, CevOss is an effective alternative to autologous bone in suitable defects.<br><br><strong>Cevoss Applications:</strong><br><ul><li>Bone defects and bone augmentation in general</li><li>Alveolar ridge augmentation/reconstruction</li><li>Socket filling post-extraction - ridge preservation</li><li>Implantology: implant site preparation, bone defect filling and maxillary sinus lift</li><li>Periodontology: bone defect filling, membrane support during guided tissue regeneration</li></ul><h2>CevOss Compares Favorably to BioOss&reg;</h2><p><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/cevoss-bone-formation.png" alt="New bone formation plot of CevOss vs Bio-Oss" class="fr-fic fr-dii"></p><p><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/cevoss-remaining.png" alt="cevoss remaining bone" class="fr-fic fr-dii"></p><br><em>1. Bio-Oss&reg; is a registered trademark of Geistlich, Wolhusen, Switzerland. Substantial equivalence of Cevoss was determined by the FDA in the<a href="https://osseonews.nyc3.digitaloceanspaces.com/ddsgadget/downloads/ODONTIT-K123876.pdf" rel="noopener  noreferrer" target="_blank">&nbsp;original 510K submission</a> by the manufacturer Odontit for Synergy Bone Matrix material. Synergy Bone Matrix is distributed by Citagenix under Trademark CevOss.&nbsp;</em>Data on file.

CevOss Bovine Bone Graft

OsseoSeal (formerly Ossguide) is a resorbable collagen membrane derived from purified porcine pericardium. This membrane was designed to provide superior barrier function, while maintaining ideal handling characteristics. Once hydrated, the Ossguide&trade; collagen membrane has excellent tensile strength and is not easily torn. This ensures that clinicians can easily stretch the membrane without tearing. &nbsp; Ossguide&trade;  is an ideal membrane for GBR procedures.
<br>
<br>

<ul>
	<li>Substantially Equivalent to BIO-GIDE&reg; <sup>1</sup> (see data below)</li>
	<li>Material: Type 1 porcine pericardium</li>
	<li>Resorption time: 3 months</li>
	<li>Fast hydration and excellent tensile strength</li>
	<li>Good adaptation to various defects</li>
	<li>Excellent tear function and duration</li>
	
</ul>

<p>Several cases showing the use of the Ossguide Membrane.</p>

Ossguide Video

<img style="float: right;" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide5.jpeg" class="fr-fic fr-dib">OsseoSeal (formerly OssGuide), is a resorbable collagen membrane derived from purified porcine pericardium. This membrane was designed to provide superior barrier function, while maintaining ideal handling characteristics. Once hydrated, the Ossguide&trade; collagen membrane has excellent tensile strength and is not easily torn. This ensures that clinicians can easily stretch the membrane without tearing. &nbsp; Ossguide&trade; the ideal membrane for tenting and a other GBR procedures.<br><h2><strong>OssGuide Indications:</strong></h2>OssGuide is recommended for:&nbsp;<ul><li>Simultaneous use of GBR-membrane (OssGuide) and implants;&nbsp;</li><li>Augmentation around implants placed in immediate extraction sockets;&nbsp;</li><li>Augmentation around implants placed in delayed extraction sockets;&nbsp;</li><li>Localized ridge augmentation for later implantation;&nbsp;</li><li>Alveolar ridge reconstruction for prosthetic treatment;&nbsp;</li><li>Aid regeneration of bone defects after root resection, cystectomy, removal of retained teeth;&nbsp;</li><li>Guided bone regeneration in dehiscence defects</li></ul><br><h2>Ossguide Resorption time</h2>In a controlled study, OssGuide maintained its contour until 8 weeks, lost most of its integrity after 12 weeks, and disappeared by biodegradation at 24 weeks.<br><br><strong>Substantially Equivalence to &nbsp;BIO-GIDE&reg;&nbsp;<br></strong>The FDA concluded in the&nbsp;<a href="https://www.accessdata.fda.gov/cdrh_docs/pdf20/K200623.pdf" rel="noopener noreferrer" target="_blank">510K submission for Ossguide</a>(K200623) that it is substantially equivalent to Bio-Guide, the predicate device used in the 510K submission. If you read the submission, it is noted that in many respects Ossguide is identical to Bio-Guide. The primary difference is that Bio-Guide is made from Porcine peritoneum, while Ossguide is manufactured from Porcine pericardium.<br><h2>Ossguide Placement</h2><br>OssGuide can be placed either dry or hydrated. OssGuide can be trimmed to the size and shape of the defect in a dry or wet state using scissors. A piece of sterile Tyvek may be used as a template for membrane sizing and trimming. OssGuide should overlap the walls of the defect by at least 2 mm to allow complete bone contact and to prevent gingival connective tissue invasion below the material. The membrane may be secured in place with sutures, tacks, or by means of sufficient contact with the mucoperiosteal flap to avoid displacement and micro motion during healing. To facilitate proper healing, ensure that there is tension-free primary closure of the soft tissue flap covering the membrane<br><br><strong>Comparison of Tensile Strength with &quot;other product&quot;</strong><br><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide6.jpeg" class="fr-fic fr-dib"><br><strong>Osteoblast Cell Adhesion Test</strong><br><br>After the cultivation by U-2OS osteoblast cell line it is confirmed osteoblast cell line, it is confirmed by SEM that bone cell is well adhered and replicated on adhered and replicated on surface of OssGuideTM in day 3.<br><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide4.jpeg" class="fr-fic fr-dib"><br><strong>Bone Volume, Bone Intensity Test (Rat&rsquo;s Calvarial Bone Defect Model)</strong><br>In reviewing the result of micro CT in rat&rsquo;s calvarial bone defect models, after 12 weeks from the operation, a bone volume of OssGuideTM is increased up to 93.15 and bone intensity is up to 1.68. In reviewing the opinion of tissue inspection, after &nbsp;12 weeks from the operation, OssGuide shows perfect bone generation<br><br><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide3.jpeg" class="fr-fic fr-dib"><br><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide2.jpeg" class="fr-fic fr-dib"><strong>Clinical Application of OssGuideTM</strong><br><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ossguide1.jpeg" class="fr-fic fr-dib"><br><br>1. BioGide&reg; is a registered trademark of Geistlich

OsseoSeal Resorbable Porcine Collagen Membrane

Acellular dermal matrix (ADM) or acellular dermis, has the natural elasticity of human skin. It is generally used for root coverage, gingival augmentation, or soft tissue augmentation around implants, when a CTG or FGG with autogenous tissue is not an option. DALI &trade; ADM, from DDSGadget, is provided by Surgenex, a leading provider of the highest quality tissue allografts.
<br>

<ul>
	<li><strong>Compare to Alloderm <sup>1</sup> and Puros Dermis<sup>1</sup></strong></li>
	<li>No Refrigeration - Store At Room Temperature&nbsp;</li>
	<li>Minimally processed to preserve the extracellular matrix</li>
	<li>Can be shaped with scissors or a scalpel</li>
	<li>Thickness approximately 0.6 mm</li>
	<li>Resorption: 3 to 4 months</li>
</ul>

Acellular dermal matrix (ADM) or acellular dermis, has the natural elasticity of human skin. It is generally used for root coverage, gingival augmentation, or soft tissue augmentation around implants, when a CTG or FGG with autogenous tissue is not an option. DALI &reg; ADM, from DDSGadget, is provided by Surgenex, a leading provider of the highest quality tissue allografts.<br><ul><li><strong>Compare to Alloderm <sup>1</sup> and Puros Dermis<sup>1</sup></strong></li><li>No Refrigeration - Store At Room Temperature&nbsp;</li><li>Minimally processed to preserve the extracellular matrix</li><li>Can be shaped with scissors or a scalpel</li><li>Thickness approximately 0.6 mm</li><li>Resorption: 3 to 4 months</li></ul><br><br>Acellular dermal matrix (ADM) or acellular dermis is a soft connective tissue graft generated by a decellularization process that preserves the intact extracellular skin matrix. Upon implantation, this structure serves as a scaffold for donor-side cells to facilitate subsequent incorporation and revascularization.<br>These human derived dermal grafts are decellularized to remove cellular components and preserve the biological properties that promote revascularization and repair. DALI &reg; ADM acellular dermis, has the natural elasticity of human skin. DALI &reg; ADM is minimally processed to remove epidermal and dermal cells while preserving the extracellular matrix of the dermis. The grafts are freeze-dried and sterilized providing at least 2 years of shelf life at room temperature. DALI&reg; ADM is available in a variety of sizes and can be shaped with scissors or a scalpel.<br>An ADM is generally used for root coverage, gingival augmentation, or soft tissue augmentation around implants, when a CTG or FGG with autogenous tissue is not an option, i.e. a secondary surgical site is not an option for a variety of reasons.<br><strong>Applications include:</strong><br><ul><li>root coverage</li><li>gingival augmentation</li><li>soft tissue augmentation around implants</li><li>soft tissue ridge augmentation</li></ul><strong>Precautions</strong><br><ul><li>DALI&reg; ADM has a distinct basement membrane and dermal surface. (See the IFU and Questions and Answers)</li><li>Do not bend DALI&reg; ADM before rehydration.</li><li>Normal rehydration of DALI&reg; ADM is usually accomplished in 20 minutes. &nbsp;</li><li>If any hair is visible, remove before implantation.</li><li>DALI&reg; ADM may be aseptically trimmed to required dimensions, if necessary.</li><li>In case of 1X1 size of DALI&reg; ADM, it does not have the Paper backing</li></ul>Available in a variety of sizes and thickness, and can be shaped with scissors or a scalpel.<br>Resorption Time:<br><ul><li>3 to 4 months (thin)</li></ul><strong>STERILIZATION</strong><br>This tissue allograft has been sterilized, via Gamma irradiation, to a SAL of 10-6 (Sterility Assurance Level). This allograft must not be sterilized or re-sterilized by your facility.<br>DO NOT RE-STERILIZE.<br><strong>Tissue Source: Surgenex</strong><br>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.<br>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).<br><small>1. Alloderm is a registered trademark of LifeCell. Puros is a registered trademark of Zimmer Biomet.</small>

DALI Acellular Dermis

Ora-Aid is an intra-oral non-eugenol dressing for protecting oral wounds, and represents a phenomenal innovation in oral wound management and care. Ora-Aid is comprised of  2 layers: an oral mucosa adhesive side and a protection side. When exposed to moisture, the adhesive side changes into a gel state to achieve adhesion to the wound area. The protection side consists of a water insoluble polymer which covers the wound to protect the applicable area from the environment in the oral cavity. 

<strong>Please watch our videos below and read the questions for additional detail on Ora-Aid</strong>
<ul>
<li>Proven technology with years of use in Europe and Asia.</li>
<li>Protects intraoral wounds from food, bacteria and other foreign substances.</li>
<li>Protects suture threads from tongue irritation</li>
<li>Protects bone graft materials and membranes</li>
<li>Reduces pain and sensitivity</li>
<li>Prevents damage to the site during initial healing period</li>
<li>Easy to cut and shape</li>
<li>Rapid healing effects by protecting the healing growth factors in exudate</li>
<li> No working time limitation or mixing required!</li>
<li>Superior esthetics! Dressing is transparent! </li>

</ul>

A quick selection of cases demonstrating the use of Ora-Aid

Ora-Aid Cases

A quick video demonstrating Ora-Aid protocol for a basic extraction site after injection of graft material (Bond Apatite in this case). It shows trimming of the Ora-Aid and placement, as well as the suturing technique required to maintain Ora-Aid at the site.

Ora-Aid Protocol for Extraction

Short lecture video explaining the benefits of Ora-Aid. Video also shows the suture technique.

Ora Aid Lecture and Suture Protocol

Short video with a graphical review of the suture protocol.

Suture Protocol

<div class="rounded-md bg-yellow-50 p-4"><div class="flex"><div class="flex-shrink-0">ⓘ</div><div class="ml-3"><h3 class="text-lg font-medium text-yellow-800">Ora-Aid Q&amp;A and Videos</h3><div class="mt-2 text-yellow-700"><p>See the tabs above for Q&amp;A on Ora-Aid and key Instructional Videos.</p></div></div></div></div><p><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-ben-2.jpeg" alt="easy to use" class="fr-fic fr-dii"><span class="mt-4 font-bold">&nbsp;ORA-AID: It is easy to use, just peel off and stick on the site</span></p><p><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-ben-1.jpeg" alt="improve" class="fr-fic fr-dii"><span class="mt-4 font-bold">&nbsp;ORA-AID: You can improve the predictability and success rate of intra oral surgery by good sealing and extra protection</span></p><div class="grid grid-cols-1 md:grid-cols-6"><br></div><h2>Ora-Aid How to Use</h2><div class="grid grid-cols-2 gap-x-4 gap-y-8 sm:grid-cols-3 sm:gap-x-6 md:grid-cols-5 xl:gap-x-8"><div class="w-full rounded"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-how-1.png" alt="Irrigate wound with sterile or saline solution" class="fr-fic fr-dii"><span class="mt-2">1. Irrigate the wound with sterile or saline solution</span></div><div class="w-full rounded"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-how-2.png" alt="Irrigate wound with sterile or saline solution" class="fr-fic fr-dii"><span class="mt-2">2. Cut Ora-Aid into a proper shape and size. It should be trimmed according to the length of surgical site. (watch our videos for a demonstration of a cutting technique)</span></div><div class="w-full rounded"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-how-3.png" alt="Slightly remove moisture with gauze on the wound." class="fr-fic fr-dii"><span class="mt-2">3. Slightly remove moisture, and excess saliva &nbsp;with gauze on the wound. Excessive moisture or exudation may reduce the adhesive strength and attachment time of Ora-Aid.</span></div><div class="w-full rounded"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-how-4.png" alt="Remove transparent release paper and apply on wound." class="fr-fic fr-dii"><span class="mt-2">4. Remove transparent release paper and apply Ora-Aid on the wound.</span></div><div class="w-full rounded"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-how-5.png" alt="5 to 10 seconds while Ora-Aid adheres to wound" class="fr-fic fr-dii"><span class="mt-2">5. Gently press Ora-Aid for 5 to 10 seconds while Ora-Aid adheres to wound.</span></div></div><br><br><br><br><strong>Ora-Aid Description</strong><br>Ora-Aid Wound Dressing is a device comprised of an oral mucosa adhesive side and a protection side. The oral mucosa adhesive side is composed of a water soluble polymer that when exposed to moisture in the oral cavity changes into a gel state to achieve adhesion to the wound area. The protection side consists of a water insoluble polymer which covers the wound to protect the applicable area from the environment in the oral cavity. Ora-Aid Wound Dressing is simply a non-sterile bandage to protect oral wounds.<br><br><strong>Ora-Aid Indications</strong><br>Ora-Aid is intended for the management of all types of oral wounds, injuries and ulcerations of the gingival and oral mucosa, including stomatitis, minor chafing and traumatic ulcers, abrasions caused by braces and ill-fitting dentures, and lesions associated with oral surgery. Ora-Aid operates to relieve pain by adhering to and protecting affected tissues from further irritation, thereby allowing healing<br><br><h3 class="text-lg">Ora-Aid Cases</h3><div class="grid grid-cols-1 gap-x-4 gap-y-8 sm:gap-x-6 md:grid-cols-3 xl:gap-x-8"><div class="w-full rounded"><span class="mt-2 mb-2">Subepithelial connective graft</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-1.png" alt="Subepithelial connective graft" class="fr-fic fr-dii"></div><div class="w-full rounded"><span class="mt-2 mb-2">Crown lengthening procedure: CLP1</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-2.png" alt="Crown lengthening procedure: CLP1" class="fr-fic fr-dii"></div><div class="w-full rounded"><span class="mt-2 mb-2">Periodontal Flap Operation</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-3.png" alt="Periodontal Flap Operation" class="fr-fic fr-dii"></div><div class="w-full rounded"><span class="mt-2 mb-2">Implantation</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-6.png" alt="Implantation" class="fr-fic fr-dii"></div><div class="w-full rounded"><span class="mt-2 mb-2">Extraction and Implantation</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-7.png" alt="Extraction" class="fr-fic fr-dii"></div><div class="w-full rounded"><span class="mt-2 mb-2">Temporary denture</span><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/ora-aid-case-8.png" alt="Temporary denture" class="fr-fic fr-dii"></div></div>

Ora-Aid : Attachable IntraOral Wound Dressing

Electric torque wrench provides accurate tightening torque while minimizing potential fracture. The right angle implant torque wrench with precise torque measure makes it easy to access implant components in difficult to reach posterior areas.

This video shows additional details for the Electric Wireless Torque Driver

Wireless Torque Video

<ul><li><strong>Prosthetic screw connection all in one</strong><ul><li>Accurate tightening torque minimizes fracture / loosing</li><li>Contra angle structure allow easy access to posterior parts</li><li>Abutment and orthodontic fixtures can be directly buried and shorten procedure time</li></ul></li><li><strong>Easy use when orthodontic mini screw inserted</strong><ul><li>5 ~ 35 Ncm for placement / removal even from hard bone</li><li>Torque setting function minimizes calibration screw fracture / fall</li></ul></li><li><strong>Accurate and quick setup</strong></li><li><strong>1 year warranty</strong></li></ul>

Electric Wireless Torque Driver

The sterile, angled disposable bone scraper always has a fresh blade, providing the easiest way to harvest bone in an atraumatic manner.

<ul>
	<li>Sharp circular blade for 360&deg; of harvesting</li>
	<li>Never a dull blade - expose a new cutting surface with 90&deg; twist of any .050 hex driver</li>
	<li>Specially Angled to allow for access to a greater number of harvesting sites.</li>
	<li>Single patient use. Individually packaged and delivered sterile.</li>
</ul>

<p>The angled bone scraper, allows harvesting of autogenous, vital bone, in large or small amounts from any surface. Autogenous bone is considered the gold standard and has several advantages over other augmentation techniques including short healing times, favorable bone quality, lower material costs, no risk of disease transmission or antigenicity, and predictability in the repair of larger defects or greater atrophy.</p><p>If you are tired of harvesting bone shavings with a scraper that won&rsquo;t stay sharp, then it&rsquo;s time you tried the Angled Bone Scraper. There&rsquo;s no easier way to precisely harvest bone in an atraumatic manner.</p><p>The 360&ordm; blade is marked into four sections. As the blade starts to dull, you can expose a new cutting surface by simply twisting the blade with any .050 hex driver. And the improved angle allows easier access to greater number of harvesting sites. If you&rsquo;ve never used an angled scraper, you won&rsquo;t believe how much easier it is to use than a straight bone scraper.&nbsp;The secret is to hold the angled Glider at a 35 degree angle on the ridge.</p><h2>Bone Scraper Features</h2><ul><li>Easy slide bone trap for bone retrieval</li><li>Collect up to 2.5cc of graft material</li><li>Sharp circular blade for 360&deg; of harvesting</li><li>Never a dull blade &ndash; expose a new cutting surface with 90&deg; twist of any .050 hex driver</li></ul><h2>Bone Scraper Benefits</h2><ul><li><strong>Ergonomic design &nbsp;and simple collection chamber</strong><br>Integrated System Rapidly Cuts, Collects And Delivers. Improved handling of harvesting graft with simple slide of bone trap, and angled to allow access to greater number of harvesting sites. Recommended for the ramus, symphasis and tuberosity areas.</li><li><strong>Bone is collected with coagulated blood&nbsp;</strong><br>Since the bone is collected with coagulated blood, it displays a high biological plasticity shortly after it is harvested. This makes the graft extremely easy to handle and mold.</li><li><strong>Superior harvesting method&nbsp;</strong><br>Since the bone scraper harvests the bone manually, the graft&#39;s cellular vitality is maintained , with no risk of potentially overheating bone. Bone shavings harvested with the angled bone scraper have the porosity and low density to allow angiogenesis.</li><li><strong>Safe</strong><br>The disposable scraper is sterile and individually packaged for single patient use. There is therefore no risk of contamination between patients, and the chance of disease transmission is eliminated. Clean up is easy and fast.</li></ul>

Disposable Bone Scraper: Angled

<p>The Universal Implant Prosthetic Driver Kit with Torque Wrench, gives you the ability to handle any implant brand attachment. Save time and money by not having to order drivers from many different companies.</p>
<p>Kit includes:</p>
<ul>
<li>1.20mm Hex Driver (Short/Long) (3i, Keystone, Hiossen/Ostem, Megagen, Dentium)</li>
<li>1.25/1.27mm Hex Driver (Short/Long) (Zimmer, Astra, Biohorizons, Intra-Lock, MIS, Implant Direct)</li>
<li>Unigrip (Short/Long) ( Nobel Biocare)</li>
<li>SCS (Short/Long) ( Straumann)</li>
<li>Adjustable Torque Wrench (10 - 40 Ncm)</li>
<li>New! Optional Convert Adapter to convert square head driver to round head to use our torque wrench.</li>
</ul>

<p>This kit is used to remove and fasten implant prosthetics. It includes a complete set of components for tightening clinical and prosthetic screws to the correct torque value.</p><h3>Prosthetic Kit Components</h3><br><div class="row"><div class="col-sm-6"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/prosthetic-driver-kit-small.png" class="fr-fic fr-dii"></div><div class="col-sm-6"><img src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/prosthetic-driver-torque.png" class="fr-fic fr-dii"></div></div><br><br><h3>Prosthetic Driver Sets</h3><br><div class="row"><div class="col-sm-3" style="font-size: .8em;line-height: 1.3em;text-align: center;"><strong>1.2 mm Hex Green <br>Long, 15mm (1)<br>Short, 10mm (1)</strong><br><img alt="mallet" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/universal-driver-3.png" class="fr-fic fr-dii"><br>(3i, Keystone, Hiossen/Ostem, Megagen, Dentium)</div><div class="col-sm-3" style="font-size: .8em;line-height: 1.3em; text-align: center;"><strong>1.25/1.27mm Blue <br>Long, 15mm (1)<br>Short, 10mm (1)</strong><br><img alt="Zimmer, Astra, Biohorizons, Intra-Lock, MIS, Implant Direct" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/universal-driver-4.png" class="fr-fic fr-dii"><br>(Zimmer, Astra, Biohorizons, Intra-Lock, MIS, Implant Direct, Sybron)</div><div class="col-sm-3" style="font-size: .8em;line-height: 1.3em;text-align: center;"><strong>ITI/SCS Purple <br>Long, 15mm (1)<br>Short, 10mm (1)</strong><br><img alt="Straumann" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/universal-driver-1.png" class="fr-fic fr-dii">(Straumann)</div><div class="col-sm-3" style="font-size: .8em;line-height: 1.3em;text-align: center;"><strong>Star/Unigrip Yellow <br>Long, 15mm (1)<br>Short, 10mm (1)</strong><br><img alt="NobelBiocare Active, <br/>Unigrip Screw, Neoss" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/universal-driver-2.png" class="fr-fic fr-dii">(NobelBiocare, Unigrip Screw, Neoss)</div></div><h3>Convert Adapter</h3>The kit also comes with a convert adapter to help convert square head driver into a round head for use with our ratchet.<br><img alt="adapter" src="https://osseonews.nyc3.cdn.digitaloceanspaces.com/ddsgadget-images/adapter.png" class="fr-fic fr-dii">