Device Name: Matriform StripIndication for Use:Matriform® Si Strip is intended t
Device Name: Matriform StripIndication for Use:Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process
Device Name: Matriform SI-StripIndication for Use:Matriform® Si Strip is intende
Device Name: Matriform SI-StripIndication for Use:Matriform® Si Strip is intended to fill bony voids or gaps of the skeletal system (posterolateral spine). These osseous defects may be surgically created or from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. In the posterolateral spine Matriform® Si Strip is to be mixed with autograft bone. The device resorbs and is replaced with bone during the healing process
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for
Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes
Device Name: Matriform LargeMofidication: Mouldable FoamIndication for Use:Matri
Device Name: Matriform LargeMofidication: Mouldable FoamIndication for Use:Matriform Large is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Matriform Large resorbs and is replaced with bone during healing process.
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm
Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR)
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:
Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo
Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process.
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use
Device Name: IngeniOS ß-TCP Bioactiv Synthetic Bone ParticlesIndications for Use:Oral and maxillofacial surgery and dentistry• Augmentation or reconstructive treatment of the alveolar ridge• Filling of infrabony periodontal defects• Filling of defects after root resection, apicoectomy, and cystectomy• Filing of extraction sockets to enhance preservation of the alveolar ridge• Elevation of the maxillary sinus floor
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistr
Device Name: IngeniOS HAIndications for Use:Oral-maxillofacial surgery, dentistry, implantology, periodontology• Defects after removal of bone cysts• Augmentation of the atrophied alveolar ridge• Sinus floor elevation (subantral augmentation)• Filling of alveolar defects following tooth extraction for alveolar ridge preservation• Filling of extraction defects to create an implant bed• Filling of two or multi-walled infrabony pockets, and bi and trifurcation defects• Support function for a membrane in guided tissue regeneration (GTR)• Defects after surgical removal of retained teeth or corrective osteotomies• Other multi-walled bone defects of the alveolar ridge
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
#ORAMEM SUS 30x40OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 30x40OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
#ORAMEM SUS 20x30OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 20x30OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
#ORAMEM SUS 15x20OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 15x20OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 30x40OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 30x40OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 20x30OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 20x30OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 15x20OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 15x20OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
BIOMEND EXTEND 30MM X 40MM (0142) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 30MM X 40MM (0142) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 30MM X 40MM (0107)BioMend Absorbable Collagen Membrane is an absorbab
BIOMEND 30MM X 40MM (0107)BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus.The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND EXTEND 20MM X 30MM (0141) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 20MM X 30MM (0141) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 20MM X 30MM (0105) BioMend Absorbable Collagen Membrane is an absorbable
BIOMEND 20MM X 30MM (0105) BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND EXTEND 15MM X 20MM (0140) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 15MM X 20MM (0140) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 15 MM X 20 MM(0103)BioMend Absorbable Collagen Membrane is an absorbabl
BIOMEND 15 MM X 20 MM(0103)BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus.The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif
HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks.