| 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 | 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 |
| 4 | 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 |
| 5 | 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 | |
| 6 | 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 | |
| 7 | 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 | |
| 8 | 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 |
| 9 | 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 | |
| 10 | 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 |
| 11 | 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 |
| 12 | 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 |
| 13 | D767U0302051 | 200-600um 1.0g | U03-0205 | 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 | |
| 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 | 00888118110411 | 50-334-06-09 | PLATE, ORTHOG, BSSO, CVD, 15 MM BRG, 2.0 MM SCREW, TI-6AL-4V | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 2 | 00888118110404 | 50-333-06-09 | PLATE, ORTHOG, BSSO, CVD, 13 MM BRG, 2.0 MM SCREW, TI-6AL-4V | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 3 | 00888118108944 | 25-197-09-71 | PLATE, L1 MMF FIXATION, 2.0 MM L1 MMF SCREW, CP TITANIUM | LEVEL ONE CMF, STERILE | KLS-MARTIN L.P. | |
| 4 | 00888118108937 | 25-197-07-71 | PLATE, L1 MMF FIXATION, 2.0 MM L1 MMF SCREW, CP TITANIUM | LEVEL ONE CMF, STERILE | KLS-MARTIN L.P. | |
| 5 | 00888118108920 | 25-197-09-09 | PLATE, L1 MMF FIXATION, 2.0 MM L1 MMF SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 6 | 00888118108913 | 25-197-07-09 | PLATE, L1 MMF FIXATION, 2.0 MM L1 MMF SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 7 | 00888118108876 | 25-198-08-71 | SCREW, MAXDRIVE, L1 MMF, DRILL FREE, TI-6AL-4V | LEVEL ONE CMF, STERILE | KLS-MARTIN L.P. | |
| 8 | 00888118108869 | 25-198-08-61 | SCREW, MAXDRIVE, L1 MMF, DRILL FREE, TI-6AL-4V | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 9 | 00888118108852 | 25-198-06-71 | SCREW, MAXDRIVE, L1 MMF, DRILL FREE, TI-6AL-4V | LEVEL ONE CMF, STERILE | KLS-MARTIN L.P. | |
| 10 | 00888118108845 | 25-198-06-61 | SCREW, MAXDRIVE, L1 MMF, DRILL FREE, TI-6AL-4V | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 11 | 00888118108821 | 25-320-35-09 | PLATE, SMART3D TRAUMA, MIDFACE, RIGHT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 12 | 00888118108814 | 25-320-34-09 | PLATE, SMART3D TRAUMA, MIDFACE, LEFT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 13 | 00888118108807 | 25-320-33-09 | PLATE, SMART3D TRAUMA, ZMC, L SHP, RIGHT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 14 | 00888118108791 | 25-320-32-09 | PLATE, SMART3D TRAUMA, ZMC, L SHP, LEFT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 15 | 00888118108784 | 25-320-31-09 | PLATE, SMART3D TRAUMA, ZMC BUTTRESS, RIGHT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 16 | 00888118108777 | 25-320-30-09 | PLATE, SMART3D TRAUMA, ZMC BUTTRESS, LEFT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 17 | 00888118108760 | 25-320-29-09 | PLATE, SMART3D TRAUMA, ZMC, L SHP, RIGHT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 18 | 00888118108753 | 25-320-28-09 | PLATE, SMART3D TRAUMA, ZMC, L SHP, LEFT, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 19 | 00888118108623 | 25-285-10-91 | PLATE, MINI, CONDYLAR, TRAPEZOID, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 20 | 00888118108609 | 99-594-33-01 | KIT, CRANIOTOMY FLAP, 25-975-03-71 (12), 25-015-05-71 (3), CP TITANIUM / TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 21 | 00888118108548 | 99-586-30-08 | PLATE, MIDFACE, LADDER, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 22 | 00888118108531 | 99-586-30-07 | PLATE, MIDFACE, CVD, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 23 | 00888118108524 | 99-586-30-06 | PLATE, MIDFACE, STR, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 24 | 00888118108517 | 99-586-30-05 | PLATE, MIDFACE, Y SHP, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 25 | 00888118108500 | 99-586-30-04 | PLATE, MIDFACE, DBL Y SHP, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 26 | 00888118108494 | 99-586-30-03 | PLATE, MIDFACE, X SHP, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 27 | 00888118108487 | 99-586-30-02 | PLATE, MIDFACE, STR, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 28 | 00888118108470 | 99-586-30-01 | PLATE, MIDFACE, STR, W/TAB, 1.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 29 | 00888118108029 | 51-610-60-91 | PIN, DRILL FREE, TI-6AL-4V | DISTRACTION, EXTERNAL | KLS-MARTIN L.P. | |
| 30 | 00888118108012 | 51-608-60-91 | PIN, DRILL FREE, TI-6AL-4V | DISTRACTION, EXTERNAL | KLS-MARTIN L.P. | |
| 31 | 00888118108005 | 51-606-60-91 | PIN, DRILL FREE, TI-6AL-4V | DISTRACTION, EXTERNAL | KLS-MARTIN L.P. | |
| 32 | 00888118107992 | 51-606-50-91 | PIN, DRILL FREE, TI-6AL-4V | DISTRACTION, EXTERNAL | KLS-MARTIN L.P. | |
| 33 | 00888118107985 | 51-606-40-91 | PIN, DRILL FREE, TI-6AL-4V | DISTRACTION, EXTERNAL | KLS-MARTIN L.P. | |
| 34 | 00888118107978 | 50-305-12-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 35 | 00888118107961 | 50-305-10-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 36 | 00888118107954 | 50-305-08-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 37 | 00888118107947 | 50-305-06-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 38 | 00888118107930 | 50-305-04-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 39 | 00888118107923 | 50-305-02-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 40 | 00888118107916 | 50-305-00-09 | PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, PLATE, ORTHOG, GENIOPLASTY, DBL Y SHP, W/TAB, INFERIOR HOLES, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 41 | 00888118107817 | 50-743-04-09 | PLATE, MINI, TLTS, Z SHP, RIGHT, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 42 | 00888118107800 | 50-742-04-09 | PLATE, MINI, TLTS, Z SHP, LEFT, 2.0-2.5 MM SCREW, CP TITANIUM | LEVEL ONE CMF | KLS-MARTIN L.P. | |
| 43 | 00888118106940 | 25-153-07-71 | PLATE, ULTRAONE, Y SHP, W/TAB, NEURO SCREW, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 44 | 00888118106933 | 25-153-01-71 | PLATE, ULTRAONE, X SHP, W/TAB, NEURO SCREW, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 45 | 00888118106926 | 25-976-05-71 | SCREW, MAXDRIVE, DRILL FREE, EMERGENCY, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 46 | 00888118106896 | 25-975-05-71 | SCREW, MAXDRIVE, DRILL FREE, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 47 | 00888118106858 | 25-975-04-71 | SCREW, MAXDRIVE, DRILL FREE, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 48 | 00888118106810 | 25-975-03-71 | SCREW, MAXDRIVE, DRILL FREE, TI-6AL-4V | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 49 | 00888118106797 | 25-153-85-71 | MESH, STANDARD, ULTRAONE, NEURO SCREW, CP TITANIUM | LEVEL ONE NEURO, STERILE | KLS-MARTIN L.P. | |
| 50 | 00888118106780 | 25-153-85-09 | MESH, STANDARD, ULTRAONE, W/TAB, NEURO SCREW, CP TITANIUM | LEVEL ONE NEURO | KLS-MARTIN L.P. |