The Screw Fixation System provides a compact solution for the temporary fixation and stabilization of bone transplants, suitable resorbable and non-resorbable bone replacement materials, and membranes for the alveolar ridge. Two color coded systems in 1.5 mmD MICRO (BLUE) and 2.0 mmD MINI (RED) offer concise and cost effective functional options. The color coding scheme for the two systems, the components and the screws, makes easy and rapid identification of the parts possible and simplifies parts matching. This modular storage system permits individual configuration and the open design ensures access during cleaning and sterilization. Fixation screws and mesh are manufactured from pure titanium or titanium alloy. They are biocompatible, corrosionproof and non-toxic in the biological environment. They allow imaging virtually free of artifacts.
Secure & Simple
The Screw Fixation System comes with power grip for secure and stable transfer to the surgical site. The screws are easily picked up and have a reliable connection to the driver.
The screw cartridges of the Screw Fixation System are more than simply storage containers. The cartridges make organization and sterilization of screws easy.
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ZB0205 - Screw Fixation System Brochure
ZB0937 - Regenerative Product Portfolio (France Only)
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 C 04/18 ©2018 Zimmer Biomet. All rights reserved.