- Tsao YP, Neiva R, Al-Shammari K, Oh TJ, Wang HL. Effects of a mineralized human cancellous bone allograft in regeneration of mandibular Class II furcation defects. J Periodontol. 2006;77:416-425.
- Keith JD Jr, Petrungaro P, Leonetti JA, Elwell CW Jr, Zeren KJ, Caputo C, et al. Clinical and histologic evaluation of a mineralized block allograft: results from the developmental period (2001-2004). Int J Periodontics Restorative Dent. 2006;26:321-327.
- Leonetti JA, Koup R. Localized maxillary ridge augmentation with a block allograft for dental implant placement: case reports. Implant Dent. 2003;12:217-226.
- Froum SJ, Wallace SS, Elian N, Cho SC, Tarnow DP. Comparison of mineralized cancellous bone allograft (Puros) and anorganic bovine bone matrix (Bio-Oss) for sinus augmentation: histomorphometry at 26 to 32 weeks after grafting. Int J Periodontics Restorative Dent. 2006;26:543-551.
- Noumbissi SS, Lozada JL, Boyne PJ, Rohrer MD, Clem D, Kim JS, Prasad H. Clinical, histologic, and histomorphometric evaluation of mineralized solvent-dehydrated bone allograft (Puros) in human maxillary sinus grafts. J Oral Implantol. 2005;31:171-179.
- Block MS, Finger I, Lytle R. Human mineralized bone in extraction sites before implant placement. Preliminary results. J Amer Dent Assoc. 2002;133:1631-1638.
- Minichetti JC, D’Amore JC, Hong AYJ, Cleveland DB. Human histologic analysis of mineralized bone allograft (Puros) placement before implant surgery. J Oral Implantol. 2004;30:74-82.
- Data on file with RTI Surgical, Inc.
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- Le B, Rohrer MD, Prassad HS. Screw “tent-pole” grafting technique for reconstruction of large vertical alveolar ridge defects using human mineralized allograft for implant site preparation. J Oral Maxillofac Surg. 68:428-435, 2010.
- Block MS, Degen M. Horizontal ridge augmentation using human mineralized particulate bone: preliminary results. J Oral Maxillofac Surg. 2004;62(Suppl 2):67-72.
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- Effect of terminal gamma sterilization on osteoinductivity. White paper available from RTI Surgical, Inc.
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- Instructions for Use.
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Changing The Concept Of Block Grafting
By eliminating the need to harvest an autogenous block graft, Puros Block Allografts may save time and help to reduce pain and can shorten the patient’s rehabilitation period.
- Shelf-life: Five (5) years
The Unique Tutoplast Process
For over 40 years, Tutoplast processed tissues have been used in more than five million procedures.8
- The Tutoplast Process is a validated chemical sterilization process that assures the highest standard of tissue safety; validated to achieve terminal sterility of SAL 10-6.8
- The process preserves the valuable collagen matrix and tissue integrity while inactivating pathogens and gently removing unwanted materials, such as cells, antigens and viruses.9,10
- A clinically documented solution for effectively restoring volume to severely resorbed ridges2,3,18
- Outcomes have been comparable to those generally reported for autogenous block grafting, but without the need for a second surgery to harvest bone19-21
- Clinical reports have documented the ability to stabilize implants 5 to 6 months after grafting2,3,18
- Retains osseoconductive properties due to the preservation of the natural bone matrix collagen and mineral composition, trabecular pattern and original porosity2,3
Manuals & Guidelines
Product clearance and availability may be limited to certain countries/regions. Please contact your local sales representative or customer service team.
Unless otherwise indicated, as referenced herein, all trademarks are the property of Zimmer Biomet; and all products are manufactured by one or more of the dental subsidiaries of Zimmer Biomet Holdings, Inc., and distributed and marketed by Zimmer Biomet Dental (and, in the case of distribution and marketing, its authorized marketing partners). Cancelle SP® is a registered trademark of RTI Surgical, Inc. Tutoplast is a registered trademark of Tutogen Medical GmbH. Safescraper is a trademark of C.G.M. S.P.A. NovaBone is a registered trademark of NovaBone Products, LLC. BioMend, BioMend Extend, CopiOs, CopiOs Extend, OsseoGuard, OsseoGuard Flex , and Socket Repair Membranes are manufactured by Collagen Matrix, Inc. Collagen Matrix is not a subsidiary of Zimmer Biomet Holdings. IngeniOs products are manufactured by Curasan AG. Safescraper is manufactured by META Advanced Medical Technology. NovaBone Dental Putty is manufactured by NovaBone Products, LLC. Puros is manufactured by RTI Surgical, Inc. CopiOs Xenograft and CopiOs Pericardium are manufactured by Tutogen Medical GmbH. RegenaVate is manufactured by RTI Surgical, Inc. RegenePro is manufactured by Syntacoll GmbH. RegenerOss Allograft Putty Plus is manufactured by Interpore Cross International with tissue provided by LifeLink Tissue Bank. (AATB Certified). Screw Fixation Kits are manufactured by Medicon e.G. Endobon is manufactured by Biomet France, Sarl. RegenerOss Allograft Particulate products are distributed by Zimmer Biomet Dental and processed by Community Tissue Services. Prior to August, 2016, distinct lots of RegenerOss Allograft Particulate products were processed by University of Miami Tissue Bank (UMTB). Orders may be fulfilled with product originating from either or both tissue establishment until depletion of UMTB stock. For additional product information, please refer to the individual product labeling or instructions for use. Product clearance and availability may be limited to certain countries/regions. This material is intended for clinicians only and does not comprise medical advice or recommendations. This material may not be copied or reprinted without the express written consent of Zimmer Biomet Dental.
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