Performs When Primary Closure Has Not Been Achieved
Clinical experience with CopiOs Extend Membrane has shown that the membrane shows no signs of inflammation or infection in cases where primary closure has not been achieved.
The exposed area is healed by soft tissue covering the exposure within a few weeks while the membrane maintains its barrier function.2,3
Features & Benefits
- Designed to conform to the defect with enough structural integrity for space maintenance
Extended Resorption Profile
- Lasts 6 to 9 months,1 designed to allow implant placement while providing ample time for regeneration
Performs Even When Primary Closure Is Not Attained
- No signs of inflammation or infection in cases where primary closure has not been achieved2,3
CopiOs Extend® Membrane Data Sheet
CopiOs Extend® Membran Synergie von Raum und Zeit
Membrana CopiOs Extend® Sinergia entre espacio y tiempo
Membrane CopiOs Extend
Membrana CopiOs Extend® Sinergia di spazio e tempo
Membrana CopiOs Extend® Sinergia de Espaço e de Tempo
Membrana CopiOs Extend® Sinergia de Espaço e de Tempo
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- Effect of terminal gamma sterilization on osteoinductivity. White paper available from RTI Surgical, Inc.
- Data on file with curasan AG.
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- Instructions for Use.
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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. ZB0011 REV D 08/20 ©2020 Zimmer Biomet. All rights reserved.
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