OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

GuidOss is made from pure Type I porcine collagen membrane. It is a resorbable collagen membrane for guided tissue and bone regenerations. The Type I collagen is obtained from porcine skin purified to avoid immunological reactions. The GuidOss membrane is manufactured by fibrillogenesis and glycation with sugar (ribose). The collagen fibers are self-assembled by the process of fibrillogenesis. The glycation is a natural process of cross-linking of collagen occurring in vivo. The glycated collagen fibers exhibit increased mechanical strength, thermal stability and increased resistance to pepsin digestion compared to non-glycated collagen.

GuidOss is made from pure Type I porcine collagen membrane. It is a resorbable collagen membrane for guided tissue and bone regenerations. The Type I collagen is obtained from porcine skin purified to avoid immunological reactions. The GuidOss membrane is manufactured by fibrillogenesis and glycation with sugar (ribose). The collagen fibers are self-assembled by the process of fibrillogenesis. The glycation is a natural process of cross-linking of collagen occurring in vivo. The glycated collagen fibers exhibit increased mechanical strength, thermal stability and increased resistance to pepsin digestion compared to non-glycated collagen.

GuidOss is made from pure Type I porcine collagen membrane. It is a resorbable collagen membrane for guided tissue and bone regenerations. The Type I collagen is obtained from porcine skin purified to avoid immunological reactions. The GuidOss membrane is manufactured by fibrillogenesis and glycation with sugar (ribose). The collagen fibers are self-assembled by the process of fibrillogenesis. The glycation is a natural process of cross-linking of collagen occurring in vivo. The glycated collagen fibers exhibit increased mechanical strength, thermal stability and increased resistance to pepsin digestion compared to non-glycated collagen.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation.

Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types,Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. The Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.

The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers.

Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation.