Membrane per siti alveolari di estrazione
Membrana Zimmer per la preservazione alveolare

Beneficio primario:

  • Zimmer Socket Repair Membrane is designed to assist wound healing in alveolar facial plate repair and residual ridge preservation following atraumatic, flapless single-root tooth extraction.

Vantaggi clinici:

  • Socket grafting can help to preserve bone volume for implant placement36
  • The socket repair procedure is a flapless technique designed to preserve natural soft-tissue architecture and vascularity37
  • Membrane is usually completely resorbed 26 to 38 weeks following surgery*

* Quando la membrana non è esposta la velocità di riassorbimento è di 26–38 settimane; qualora venga lasciata esposta, il tempo di riassorbimento sarà inferiore.

 

 

 

 

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ZB0937 - Regenerative Product Portfolio (France Only)

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English - EMEA

36. Sclar AG. Ridge preservation for optimum esthetics and function: the “Bio-Col” technique. Postgraduate Dentistry. 1999;6:3-11.
37. Elian N, Cho SC, Froum S, Smith RB, Tarnow DP. A simplified socket classification and repair technique. Pract Proced Aesthet Dent. 2007;19:99-104, quiz 106.
 

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  articulate 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 C 04/18 ©2018 Zimmer Biomet. All rights reserved.