RegenerOss® Synthetic

1. Cornelini R, Cangini F, Martuscelli G, Wennstrom J. Deproteinized bovine bone and biodegradable barrier membranes to support healing following immediate placement of transmucosal implants: a short-term controlled clinical trial. Int J Periodontics Restorative Dent 2004; 24:555-563
2. Rey, C., Renugopalakrishnan, V., Collins, B. and Glimcher, M., Fourier transform infrared spectroscopic study of the carbonate ions in bone mineral during aging. Calcif. Tissue Int., 1991, 49, 251–258.
3. Landi E, Celotti G, Logroscino G, Tampieri A. Carbonated hydroxyapatite as bone substitute. J Eur Cer Soc 2003;23: 2931–2937.
4. Doi Y, Shibutani T, Moriwaki Y, Kajimoto T, Iwayama Y. Sintered carbonate apatites as bioresorbable bone substitutes. J Biomed Mater Res 1998;39:603–610.
5. Hasegawa M, Doi Y, Uchida A. Cell-mediated bioresorption of sintered carbonate apatite in rabbits. J Bone Joint Surg [Br] 2003;85:142–147.
6. Data on File with Collagen Matrix, Inc.
7. X-rays should be taken to confirm the bone integrity prior to dental implant placement.

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). RegenerOss® Synthetic Mineral Collagen Composite Bone Graft is manufactured by Collagen Matrix, Inc. Collagen Matrix, Inc. is not a subsidiary of Zimmer Biomet Holdings, Inc. 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.