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Osbone® – Guideline
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Osbone® – Guideline

Osbone® – Guideline
1 /12Pages

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Osbone® – Guideline-1

Osbone® – the safe alternative for happy patients

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Osbone® – Guideline-2

Dear Dentist, Developing an effective solution for happy patients while maintaining respect for patient safety, is the foundation of all curasan products. Osbone® is a synthetic, open-cell cancellous bone replacement material for filling bone defects. It is the alternative to hydroxyapatites of allogeneic or xenogeneic origin and eliminates the risk of infections and allergic reactions. As a synthetic manufactured material Osbone® provides you with a consistent level of quality. Learn more about the use, application and added value of this innovative and safe treatment option. Still have questions? Your...

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Osbone® – Guideline-3

Osbone® − synthetic bone replacement material + eliminates the risk of allergic reactions and infections + hydroxyapatite + high degree of purity and consistent quality For use in dental medicine, implantology, periodontology as well as oral and maxillofacial surgery. Osbone® – improving patient safety. Eliminates infection and allergy risks.

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Osbone® – Guideline-4

„The safety and predictability of the treatment are top priorities. This is why Osbone®, as a synthetic hydroxyapatite for bone augmentation, has been my treatment of first choice for many years.“ Dr. Kay Pehrsson, dentist at the Haranni Clinic, Herne, Germa

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Osbone® – Guideline-5

Osbone® − the compelling alternative + eliminates the risk of infections and allergies. + increases patient confidence with a synthetic alternative to allografts or xenografts. + simplifies informed consent obligations. Osbone® – for improved patient safety. Eliminates infection and allergy risks.

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Osbone® – Guideline-6

„The new bone replacement material Osbone® is particularly suitable for use in indications that call for increased mechanical stability, because it offers the best possible structures for osseointegration and is characterised by low absorption kinetics and excellent biocompatibility.“1 Complete osseointegration of Osbone® for a stable and functional implant bed. Osbone® for filling defects and bone augmentation + for an optimal osteoconductive scaffold + for long-lasting volume stability + for large-volume augmentat

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Osbone® – Guideline-7

Best practice sinus lift surgery 1 Prepared, exposed defect 2 collagen membrane Osgide® 3 Loose filling of the defect 4 Closure of the bone window with membrane 5 Saliva-proof wound closure picture credits: Prof. NYU Dr. Ady Palti, Baden-Baden Osbone® – improving patient safety. Eliminates infection and allergy risks

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Osbone® – Guideline-8

„It was demonstrated that the specific ALP activity of the cells increases throughout the entire cultivation period. The studied material Osbone® is thus able to support not only the adhesion and proliferation, but also the osteogenic differentiation of human osteoblasts.“2 Osbone® after 1 day of cell culture Osbone® after 28 days of cell culture picture credits: Dr. Kay Pehrsson, Herne Osbone® and bovine hydroxyapatite in comparison: Good cell colonisation of Osbone® Isolated cell formation on bovine hydroxyapatite

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Osbone® – Guideline-9

Clinical experience picture credits: Dr. Kay Pehrsson, Herne In a prospective, multicentre trial3 with 190 patients, Osbone® was found to have excellent biocompatibility and osseointegration with low absorption kinetics. It is particularly suitable for use in indications that call for increased mechanical stability. External sinus lift. Complete filling of the defect with Osbone® Six months post-operatively, prior to re-entry and final treatment: good osseointegration of the implants (residual granules visible at site 26). Osbone® – the safe alternative for satisfied patients. Clinical experien...

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Osbone® – Guideline-10

Osbone® product properties synthetic El phase purity (> 95 %) El polygonally shaped granules El open-cell porous Grain size Content Item number Item no. mds Osbone® Grain size small Osbone® Grain size large

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Osbone® – Guideline-11

Holweg A, Lerner H, Pehrsson K (2012): Synthetisches Hydroxylapatit in der Dental-Chirurgie. (Ergebnisse einer offenen prospektiven multizentrischen Studie mit 190 Patienten). teamwork J Cont Dent Educ 2012, 5, 419-425. Peters F, Bernhardt A, Lode A, Gelinsky M (2010): Osbone® eine neue, synthetische Biokeramik für den Knochenersatz. Regen. Med. 2010; 3 (1): 18-22. Keller U (2011): Implantation mit simultaner vestibulärer Alveolarkammaugmentation. ZMK Juli/August 2011, Sonderausgabe: 27: 26-29. Ludwig A (2011): Knochenaufbau- und Regeneration mit einem synthetischen Hydroxylapatit. Implantologie...

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Osbone® – Guideline-12

curasan Regenerative Medicine

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