| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | D767C0245010 | M4-500 | C02-4501 | Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. | JEY | Plate, Bone | 2 | Cytoflex Mesh |
| 2 | D767C0244010 | M4-400 | C02-4401 | Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. | JEY | Plate, Bone | 2 | Cytoflex Mesh |
| 3 | D767C0243010 | M4-300 | C02-4301 | Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. | JEY | Plate, Bone | 2 | Cytoflex Mesh |
| 4 | D767C0242010 | M4-200 | C02-4201 | Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. | JEY | Plate, Bone | 2 | Cytoflex Mesh |
| 5 | D767C0241010 | M4-100 | C02-4101 | Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. | JEY | Plate, Bone | 2 | Cytoflex Mesh |
| 6 | D767B0103081 | C-003 | B01-0308 | BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. | MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | BenaCel | |
| 7 | D767B0102121 | C-002 | B01-0212 | BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. | MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | BenaCel | |
| 8 | D767B0105101 | C-005 | B01-0510 | BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. | MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | BenaCel | |
| 9 | D767B0104081 | C-004 | B01-0408 | BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation. BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. | MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | U | BenaCel |
| 10 | D767B0101081 | C-001 | B01-0108 | BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. | MGQ | Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic | BenaCel | |
| 11 | D767C0302010 | 20x25mm | C03-0201 | Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Resorb |
| 12 | D767C0301010 | 30x40mm | C03-0101 | Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Resorb |
| 13 | D767C0303010 | 12x24mm | C03-0301 | Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Resorb |
| 14 | D767U0301051 | 200-600um 0.4g | U03-0105 | Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. | LYC | Bone Grafting Material, Synthetic | Unigraft | |
| 15 | D767U0102051 | 200-400um 1.0g | U01-0205 | Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. | LYC | Bone Grafting Material, Synthetic | Unigraft | |
| 16 | D767U0101051 | 200-400um 0.4g | U01-0105 | Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. | LYC | Bone Grafting Material, Synthetic | Unigraft | |
| 17 | D767C0103010 | TEF-001 | C01-0301 | Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Smooth Tef-Guard |
| 18 | D767C0101010 | TEF-002 | C01-0101 | Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Smooth Tef-Guard |
| 19 | D767C0402010 | TEX-200 | C04-0201 | Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE), the textured version of Cytoflex® Tef-Guard® has superficial macro texture overlapping the micro pore texture on both surfaces. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. The macro texture provides additional grips for flap attachment. | NPK | Barrier, Synthetic, Intraoral | Cytoflex Textured Tef-Guard | |
| 20 | D767C0401010 | TEX-100 | C04-0101 | Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE), the textured version of Cytoflex® Tef-Guard® has superficial macro texture overlapping the micro pore texture on both surfaces. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. The macro texture provides additional grips for flap attachment. | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoflex Textured Tef-Guard |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 50601557102282 | BG4-10 | BG4-10 | fortoss® VITAL is a simple to use, synthetic, resorbable material containing pur fortoss® VITAL is a simple to use, synthetic, resorbable material containing pure ß Tri-Calcium Phosphate (ß TCP) and Calcium Sulfate. When mixed with the solution the ß TCP/Calcium Sulfate matrix produces a mouldable cohesive paste. ß Tri-Calcium Phosphate act as a scaffold through which new bone grows. The Calcium Sulfate hinders soft tissue ingrowth. Its resorption provides a calcium source early in the regenerative process. The product does not contain any animal tissue | fortoss® VITAL | BIOCOMPOSITES LTD |
| 2 | 50601557102114 | BG4-05 | BG4-05 | fortoss® VITAL is a simple to use, synthetic, resorbable material containing pur fortoss® VITAL is a simple to use, synthetic, resorbable material containing pure ß Tri-Calcium Phosphate (ß TCP) and Calcium Sulfate. When mixed with the solution the ß TCP/Calcium Sulfate matrix produces a mouldable cohesive paste. ß Tri-Calcium Phosphate act as a scaffold through which new bone grows. The Calcium Sulfate hinders soft tissue ingrowth. Its resorption provides a calcium source early in the regenerative process. The product does not contain any animal tissue | fortoss® VITAL | BIOCOMPOSITES LTD |
| 3 | 42604764313268 | 1-2mm | 1x2cc | 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 | IngeniOS HA | CURASAN AG |
| 4 | 42604764313190 | 1-2mm | 1x1cc | 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 | IngeniOS HA | CURASAN AG |
| 5 | 42604764313022 | 1-2mm | 1x0.5cc | 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 | IngeniOS HA | CURASAN AG |
| 6 | 42604764312346 | 0.25-1mm | 1x2cc | 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 | IngeniOS HA | CURASAN AG |
| 7 | 42604764312278 | 0.25-1mm | 1x1cc | 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 | IngeniOS HA | CURASAN AG |
| 8 | 42604764312100 | 0.25-1mm | 1x0.5cc | 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 | IngeniOS HA | CURASAN AG |
| 9 | 42604764312032 | 0.25-1mm | 1x0.25cc | 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 | IngeniOS HA | CURASAN AG |
| 10 | 14548161312172 | 014364 | 014364 | Cytrans Granules M 2g 1pc. 231.00 | Cytrans Granules | GC AMERICA INC. |
| 11 | 14548161312165 | 014363 | 014363 | Cytrans Granules M 0.5g 1pc. | Cytrans Granules | GC AMERICA INC. |
| 12 | 14548161312158 | 014362 | 014362 | Cytrans Granules S 0.5g 1pc. | Cytrans Granules | GC AMERICA INC. |
| 13 | 14548161312141 | 014361 | 014361 | Cytrans Granules M 0.25g 1pc. | Cytrans Granules | GC AMERICA INC. |
| 14 | 14548161312134 | 014360 | 014360 | Cytrans Granules S 0.25g 1pc. | Cytrans Granules | GC AMERICA INC. |
| 15 | 10887587060941 | 710.050.98S | 71005098S | CHRONOS(TM) BETA-TCP WEDGE 10 DEG/RECTANGULAR-STERILE | ChronOS | SYNTHES GMBH |
| 16 | 10887587060934 | 710.047.98S | 71004798S | CHRONOS(TM) BETA-TCP BLOCK 20MM X 20MM X 10MM-STERILE | ChronOS | SYNTHES GMBH |
| 17 | 10887587060910 | 710.042.98S | 71004298S | CHRONOS(TM) BETA-TCP BLOCK 5MM X 5MM X 10MM-STERILE | ChronOS | SYNTHES GMBH |
| 18 | 10887587060798 | 710.014.98S | 71001498S | CHRONOS(TM) BETA-TCP GRANULES 1.4-2.8MM/5.0CC-STERILE | ChronOS | SYNTHES GMBH |
| 19 | 10887587060767 | 710.002.98S | 71000298S | CHRONOS(TM) BETA-TCP GRANULES 0.7-1.4MM/1.0CC-STERILE | ChronOS | SYNTHES GMBH |
| 20 | 10887587060750 | 710.001.98S | 71000198S | CHRONOS(TM) BETA-TCP GRANULES 0.7-1.4MM/0.5CC-STERILE | ChronOS | SYNTHES GMBH |
| 21 | 10813954024681 | FULFILL-10x20-PKG-5 | Socket Preservation Plug 10mm x 20mm | SALVIN FULFILL | COLLAGEN MATRIX, INC. | |
| 22 | 10813954024674 | FULFILL-6x25-PKG-5 | Socket Preservation Plug 6mm x 25mm | SALVIN FULFILL | COLLAGEN MATRIX, INC. | |
| 23 | 10813954024582 | 070.052 | Carbonate Apatite Plug 6mm x 25mm | Straumann SocketPlug | COLLAGEN MATRIX, INC. | |
| 24 | 10813954024575 | 070.051 | Carbonate Apatite Plug 10mm x 20mm | Straumann SocketPlug | COLLAGEN MATRIX, INC. | |
| 25 | 10813954024544 | PRPSLM | Bone Graft Composite Plug 6mm x 25mm | PreservaRidge™ Plug | COLLAGEN MATRIX, INC. | |
| 26 | 10813954024407 | PRPREG | Bone Graft Composite Plug 10mm x 20mm | PreservaRidge™ Plug | COLLAGEN MATRIX, INC. | |
| 27 | 10813954024292 | OGP1020 | Bone Graft Composite Plug 10mm x 20mm | OsteoPlug™ | COLLAGEN MATRIX, INC. | |
| 28 | 10813954024285 | OGP0625 | Bone Graft Composite Plug 6mm x 25mm | OsteoPlug™ | COLLAGEN MATRIX, INC. | |
| 29 | 10813954024278 | XA120 | Bone Graft Composite Plug | OsteoMaxx Plug | COLLAGEN MATRIX, INC. | |
| 30 | 10813954024261 | XA625 | Bone Graft Composite Plug | OsteoMaxx Plug | COLLAGEN MATRIX, INC. | |
| 31 | 10813954024230 | 5824-413 | Bone Graft Composite Plug | Gibson Healthcare® Bone Graft Plug | COLLAGEN MATRIX, INC. | |
| 32 | 10813954024223 | 5824-404 | Bone Graft Composite Plug | Gibson Healthcare® Bone Graft Plug | COLLAGEN MATRIX, INC. | |
| 33 | 10813110026733 | 260-400-525 | 260-400-525 | 0.25g SynthoGraft (500-1000um) | SynthoGraft | BICON, LLC |
| 34 | 10813110026726 | 260-400-502 | 260-400-502 | 2.0g SynthoGraft (500-1000um) | SynthoGraft | BICON, LLC |
| 35 | 10813110026719 | 260-400-501 | 260-400-501 | 1.0g SynthoGraft (500-1000um) | SynthoGraft | BICON, LLC |
| 36 | 10813110026702 | 260-400-500 | 260-400-500 | 0.5g SynthoGraft (500-1000um) | SynthoGraft | BICON, LLC |
| 37 | 10813110026696 | 260-400-152 | 260-400-152 | 2.0g SynthoGraft (50-500um) | SynthoGraft | BICON, LLC |
| 38 | 10813110026689 | 260-400-151 | 260-400-151 | 1.0g SynthoGraft (50-500um) | SynthoGraft | BICON, LLC |
| 39 | 10813110026672 | 260-400-150 | 260-400-150 | 0.5g SynthoGraft (50-500um) | SynthoGraft | BICON, LLC |
| 40 | 10813110026665 | 260-400-125 | 260-400-125 | 0.25g SynthoGraft (50-500um) | SynthoGraft | BICON, LLC |
| 41 | 10810051880066 | HA90D Small (0.3 – 1.0 mm) 3.0 cc | HA90D30S | 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 | OSTEOGENE TECH CORP |
| 42 | 10810051880059 | HA90D Small (0.3 – 1.0 mm) 1.0 cc | HA90D10S | 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 | OSTEOGENE TECH CORP |
| 43 | 10810051880042 | HA90D Small (0.3 – 1.0 mm) 0.5 cc | HA90D05S | 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 | OSTEOGENE TECH CORP |
| 44 | 10810051880035 | HA90D Large (0.8 – 1.8 mm) 3.0 cc | HA90D30L | 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 | OSTEOGENE TECH CORP |
| 45 | 10810051880028 | HA90D Large (0.8 – 1.8 mm) 1.0 cc | HA90D10L | 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 | OSTEOGENE TECH CORP |
| 46 | 10810051880011 | HA90D Large (0.8 – 1.8 mm) 0.5 cc | HA90D05L | 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 | OSTEOGENE TECH CORP |
| 47 | 10705034195926 | 276160010 | 276160010 | HEALOS ll BONE GRAFT SUBSTITUTE 10cc | HEALOS | DEPUY SPINE, LLC |
| 48 | 10705034195636 | 276050100 | 276050100 | SYMPHONY GRAFT DELIVERY SYSTEM MANIFOLD KIT | SYMPHONY | DEPUY SPINE, LLC |
| 49 | 10705034195629 | 276050000 | 276050000 | SYMPHONY GRAFT DELIVERY SYSTEM STANDARD KIT | SYMPHONY | DEPUY SPINE, LLC |
| 50 | 10381780072621 | #ORAMEMSUS30X40 | #ORAMEMSUS30X40 | #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. | Salvin OraMem® | INTEGRA LIFESCIENCES CORPORATION |