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DBM Putty

Last Updated: 6/16/2022
Brand:DCI Donor Services

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Regular Price: $99.00
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DBM Putty, from DCI Donor Services Tissue Bank, offers enhanced regenerative capacity, and superior handling, by using a proprietary combination of demineralized cortical fibers and demineralized cortical particulate.

  • New! Now available with curved syringe for better site access!
  • Reficio DBM is Made from 100% demineralized human bone – no carriers, fillers or binding agents.
  • Osteoconductive and Osteoinductive 
  • Robust Handling and Optimized Regenerative Capacity.
  • Easy storage at ambient room temperature
  • Ready for immediate use: no prep time or reconstitution required
  • Donor recovery and screening performed according to AATB and FDA guidelines
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More Information on DBM Putty

Reficio DBM Putty Video

(Note: Video shows 10.0 CC Putty for demonstration purposes. For dental applications only 1CC is currently available).

Key Benefits of DCI Donor Services Tissue Bank’s Reficio 100® DBM Putty

  • Made from 100% demineralized human bone maximizing allograft content and eliminating the need for extraneous carriers, fillers, or binding agents.
  • Osteoconductive – DBM provides an ideal scaffold that directs and supports bone formation
  • Osteoinductive – the osteoinductive potential of DBM is well established
  • Optimal regenerative capacity through a proprietary combination of demineralized cortical fibers and demineralized cortical particulate. DCI Donor Services Tissue Bank’s advanced fiber technology combines the regenerative capacity of interconnected fibers with the maximum availability of growth factors endogenous to cortical bone.
  • Excellent handling characteristics – will shape and conform to fill unique bony voids – retains shape and will not wash away or migrate
  • Easy storage and use – stores at ambient room temperature and Ready to use directly out of packaging with no need for graft preparation or hydration
  • Sterile; Sterility Assurance Level of 10-6 through low dose, low temperature gamma irradiation
  • Donor recovery and screening performed according to AATB and FDA guidelines

DCI Donor Services Tissue Bank is a non-profit, industry-leading allograft provider setting the standard in tissue quality and safety. Our dedicated team of professionals provide an extraordinary commitment to science, health and hope serving to link the gift of donation to saving and enhancing patient lives. This uncompromising, patient-centered focus generates allografts ideally suited for optimal results in a variety of surgical applications.

Commitment to Quality

The advanced tissue processing and robust quality systems employed by DCIDS Tissue Bank ensure each allograft meets stringent safety and regulatory requirements. Quality standards are established to meet or exceed regulations established by the U.S. Food and Drug Administration (FDA), standards of accredited tissue banks, and other state guidelines as appropriate. DCIDS Tissue Bank uses CLIA-certified testing laboratories for serology and microbiological testing and processes tissue in ISO Class 5 clean rooms designed with HEPA-filtered and environmentally and microbiologically monitored air. Reagents, equipment, instruments, and packaging materials used in processing meet the same standards as those used in the operating room.

Donor Selection and Screening

DCI Donor Services maintains intimate control of donor selection and procurement through its federally licensed organ procurement territories. Potential donors originating in Tennessee, New Mexico, Sacramento, and Reno are evaluated against the strict, pre-established eligibility criteria and transported to the Nashville facility for processing. This unsurpassed control and stringent criteria ensures the highest level of tissue quality and safety in the industry.

DCI Donor Services Tissue Bank’s robust quality systems are built into every stage of allograft production starting with donor screening and eligibility determination. Quality standards are established to meet or exceed the regulations and guidelines of the U.S. Food and Drug Administration, the American Association of Tissue Banks, and individual state health departments.

Processing begins with a comprehensive donor screening procedure that includes behavioral and lifestyle risk assessments, medical and social history evaluations, and a detailed physical assessment. Extensive microbiological testing is conducted to further reduce the risk of disease transmission. Tissue samples are evaluated by a CLIA certified, FDA registered laboratory for the following:

  • HIV-I & II Antibodies 
  • Hepatitis B surface antigen
  • Hepatitis B core total antibody 
  • Hepatitis C antibody 
  • HIV-I, HBV, and HCV nucleic acid test
  • Syphilis antibody
  • Aerobic and anaerobic microbiological cultures

Only donors non-reactive or negative for all testing are considered for transplantation and final donor eligibility is determined by licensed medical director.

Tissue Processing and Release

DCI Donor Services Tissue Bank’s advanced tissue processing procedures maximize the gift of donation while assuring safety and quality. Allografts are processed in accordance with current Good Tissue Practices in a class 100 clean room under stringent aseptic technique compliant with AORN standards. A combination of biological detergents work in conjunction with biocompatible, aqueous solvents and antibiotic solutions to effectively clean and disinfect allografts without compromising the tissue’s native biomechanical and biochemical properties. Procedures are validated to ensure allografts meet stringent release criteria with quality assurance inherently built into every step of the process. Independent testing has demonstrated the process: 

  • Eliminates essentially all blood elements, bone marrow, and lipids from allografts 
  • Disinfects the tissue against a panel of clinically relevant bacterial, fungal, and viral pathogens 
  • Removes residual processing agents to safe and biocompatible levels

Following processing, allografts are subjected to terminal sterilization or aseptic testing according to the specific allograft specifications. (Note: The DBM Putty is a sterile graft, and hence is subjected to low-dose, gamma irradiation.)

  • Sterile allografts are subjected to low-dose, gamma irradiation validated to Sterility Assurance Level (SAL) of 10 -6.
  • Aseptic grafts are subjected to USP <71> lot release microbiological testing including sampling 10% of the grafts produced for each donor and performing swab cultures on 100% of the final product.

Only allografts producing no microbial growth are consider for distribution and transplantation. Finally, a comprehensive review of the processing records, labeling documentation, and donor eligibility charts, are completed by a dedicated quality associate prior to the tissue being released to distribution.

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