Puros® Dermis Allograft Tissue Matrix

1. 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.
2. 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.
3. Leonetti JA, Koup R. Localized maxillary ridge augmentation with a block allograft for dental implant placement: case reports. Implant Dent. 2003;12:217-226.
4. 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.
5. 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.
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7. 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.
8. Data on file with RTI Surgical, Inc.
9. Davi E, Aslan M, Simsek G, Yilmaz AB. The effects of bone chips dehydrated with surgical solvent on healing bone defects. JIMR. 2002;30:168-173.
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15. Park SH, Wang HL. Mucogingival pouch flap for sandwich bone augmentation: technique and rationale. Implant Dent. 2005;14:349-356.
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17. Rubio de Rezende ML, Nasciemento de Melo LG, Hamata MM, Monteiro-Amado F. Particulate inlay nasal graft with immediate dental implant placement in a patient with repaired alveolar cleft; case report. Implant Dent. 2008;17:332-338.
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23. Effect of terminal gamma sterilization on osteoinductivity. White paper available from RTI Surgical, Inc.
24. Data on file with curasan AG.
25. Pietak AM, Reid JW, Stott MJ, Sayer M. Silicon substitution in the calcium phosphate bioceramics. Biomaterial. 28 (2008) 4023-4032.
26. C. Knabe, P. Ducheyne. Chapter 6 – Cellular response to bioactive ceramics, In: Handbook of Bioceramics and their Applications. Ed: Prof. Dr. Tadashi Kokubo, Woodhead Publishing Inc., Cambridge, UK, 2008, p.133-164.
27. Greenspan DC, Hernandez R, Faleris J. Histology of surgically implanted Tutoplast processed dermis; RTI Surgical, Inc.
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29. Petrungaro P. Acellular dermal matrix tissue grafts. Inside Dentistry. 2010;6:34-42.
30. Li ST, Chen HC, Lee NS, Ringshia R, Yuen D. A Comparative Study of Zimmer BioMend and BioMend Extend Membranes Made at Two Different Manufacturing Facilities. Zimmer Dental White Paper: 2013.
31. Wang HL, Carrol WJ. Guided bone regeneration using bone grafts and collagen membranes. Implant Dent. 2001;32(7):504-515.
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38. Data on file with Collagen Matrix, Inc.
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43. Data on file with Collagen Matrix, Inc.
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45. Instructions for Use.
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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. ZB0011 REV D 08/20 ©2020 Zimmer Biomet. All rights reserved.