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Universal Hand Driver
COLTENE/WHALEDENT INC
L590
In Commercial Distribution
- D661L5900 ()
- Pin/post dental drill bit
Height Adjustable Driver
L&K BIOMED CO. ,LTD.
CM0064-PT01-0002
In Commercial Distribution
- 08809986468345 ()
- Orthopaedic prosthesis implantation positioning instrument, reusable
Screw Driver
L&K BIOMED CO. ,LTD.
CM0061-CP02-0601
In Commercial Distribution
- 08809986468314 ()
- Orthopaedic prosthesis implantation positioning instrument, reusable
MIS Cannulated Screw Driver
L&K BIOMED CO. ,LTD.
LS05-2402
In Commercial Distribution
- 08809986466488 ()
- Orthopaedic prosthesis implantation positioning instrument, reusable
Height Adjustable Driver
L&K BIOMED CO. ,LTD.
BT01-0002
In Commercial Distribution
- 08809986466440 ()
- Orthopaedic prosthesis implantation positioning instrument, reusable
The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
METICULY COMPANY LIMITED
MF-314
In Commercial Distribution
- 18859751213141 ()
- 08859751213144 ()
- Craniofacial fixation plate, non-bioabsorbable, non-customized
The METICULY Patient-specific titanium maxillofacial mesh implant is a device designed individually for each patient and intended for use in selective trauma of the maxillofacial skeleton, maxillofacial surgery, and reconstructive procedures. It is specifically designed with a focus on applications of non-bending related scenarios. The implant is made of titanium alloys produced via additive manufacturing (Laser Powder Bed Fusion) and is intended to be used with titanium screws. All additive manufacturing and other post processing steps are only to take place under Meticuly manufacturing control. The device is not intended to substitute for bone reconstruction in clinical situations where bone is needed for support and stability of the maxillofacial skeleton under functional loading conditions. It is intended for adults only (at least 22 years of age). The surgeon approves the design of the mesh implant prior to fabrication of the implant device by the sponsor. The proposed FaciMesh models are intended to treat the maxillofacial region, while the OrbiMesh models treat the Orbital region. The device is not intended for reconstruction of the orbital roof defects or for any frontal bone defects, such as the supra-orbital ridge. Additionally, the FDA-cleared commercially available titanium screws that can be used with the subject devices include the TITANIUM MINIPLATE SYSTEM (K951690) and MICRO TITANIUM PLATE SYSTEM (K951688).
METICULY COMPANY LIMITED
MF-312
In Commercial Distribution
- 18859751213127 ()
- 08859751213120 ()
- Craniofacial fixation plate, non-bioabsorbable, non-customized
Single-Use Surgical Tool
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
52260
Not in Commercial Distribution
- 09008737522605 ()
- Surgical screwdriver, single-use
Single-Use Surgical Tool
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
52790
In Commercial Distribution
- 09008737527907 ()
- Surgical screwdriver, single-use
T-25 Drive Shaft, Long
Altus Spine, LLC
908-0052
In Commercial Distribution
- 00843210134611 ()
- Surgical screwdriver, reusable