Name: DALI DBM Putty
Brand: DALI
SKU: DBM-PUTTY-DCI-25800238-25803538
Price: 150 USD
Availability: InStock

DALI One Graft Plug

Dental Face Shield

DALI DBM Putty offers enhanced regenerative capacity, and superior handling, by using a proprietary process to produce demineralized bone matrix made from 100% allograft. No carriers or synthetics!
<ul>
 <li>Available with Curved Syringe for better site access!</li>
 <li>DALI DBM is Made from 100% demineralized human cortical bone &ndash; no carriers, fillers or binding agents.</li>
 <li>Osteoconductive and Osteoinductive&nbsp;</li>
 <li>Exceptional Handling and Optimized Regenerative capacity.</li>
 <li>Easy storage at ambient room temperature</li>
 <li>Ready for immediate use: no prep time or reconstitution required</li>
 <li>Donor recovery and screening performed according to AATB and FDA guidelines. </li><li>Sterilized with low-dose, gamma irradiation to a Sterility Assurance Level (SAL) of 10-6.</li>
</ul>

DALI DBM Putty is a cutting-edge demineralized bone matrix allograft,crafted to boost regeneration in dental procedures. DALI TM allograft stands for reliability and clinical excellence. Made from 100% human cortical bone, DALI DBM offers exceptional handling without carriers or synthetics. Harnessing the natural osteoconductive power of bone, DALI DMB ensures optimal bone formation, given clinicians a dependable, and cost-effective solution for superior bone grafting results.<h2>Key Benefits of DALITM DBM Putty</h2><ul><li>Made from 100% demineralized human bone maximizing allograft content and eliminating the need for extraneous carriers, fillers, or binding agents.</li><li>Osteoconductive &ndash; DBM provides an ideal scaffold that directs and supports bone formation</li><li>Osteoinductive &ndash; the osteoinductive potential of DBM is well established. DBM contains abundant bone morphogenetic proteins known to be essential for bone growth and regeneration.</li><li>Excellent handling characteristics &ndash; will shape and conform to fill unique bony voids &ndash; retains shape and will not wash away or migrate</li><li>Easy storage and use &ndash; stores at ambient room temperature and Ready to use directly out of packaging with no need for graft preparation or hydration</li><li>Sterile; Sterility Assurance Level of 10-6 through low dose, low temperature gamma irradiation</li><li>Donor recovery and screening performed according to strict AATB and FDA guidelines</li></ul>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® is an industry leading biopharmaceutical company, providing regenerative medicine solutions that set the industry standard in quality and safety. Surgenex® uses its patented Excellion® process to produce minimally manipulated products that adhere to strict regulatory standards. Following these standards allows Surgenex® 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® 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, the graft should not be used in patients with:
• Osteomyelitis at the surgical site
• Metabolic diseases (diabetes, hyperparathyroidism, osteomalacia)
• Severe renal dysfunction
• Severe liver disease
• High-dose therapy with corticosteroids
• Vascular impairment at the implant site
Warnings
• Discard grafts when mishandled, or when possible contamination of the graft has occurred.
• Return to the supplier, any package in which the sterile barrier has been compromised.
• Do not re-sterilize.
• Unused bone should be properly discarded.
• Single patient use only.
Precautions:
• Federal law (USA) restricts use to licensed clinicians
Handling 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:
• Store at ambient temperature
• 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.

DALI DBM Putty

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