Profile: Genetis S.A. are providers of craniofacial implants, dorsal nasal implants, mandibular implants, proplast ii block implant material, maxillofacial prostheses, malar implants and internal chin prostheses. All these products are available in different sizes.
7 Products/Services (Click for related suppliers)
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| • Internal Chin Prosthesis (FDA Code: FWP / 878.3550) A chin prosthesis is a silicone rubber solid device intended to be implanted to augment or reconstruct the chin. |
| • Internal Nose Prosthesis (FDA Code: FZE / 878.3680) A nose prosthesis is a silicone rubber solid device intended to be implanted to augment or reconstruct the nasal dorsum. |
| • Malar Implants (FDA Code: LZK / 878.3550) |
| • Mandibular Implant Facial Prosthesis (FDA Code: JAZ / 874.3695) A mandibular implant facial prosthesis is a device that is intended to be implanted for use in the functional reconstruction of mandibular deficits. The device is made of materials such as stainless steel, tantalum, titanium, cobalt-chromium based alloy, polytetrafluoroethylene, silicone elastomer, polyethylene, polyurethane, or polytetrafluoroethylene with carbon fibers composite. |
| • Maxillofacial Prosthesis |
| • Non-Alterable Preformed Skull Bone Plate (FDA Code: GXN / 882.5330) A preformed nonalterable cranioplasty plate is a device that is implanted in a patient to repair a skull defect and is constructed of a material, e.g., stainless steel or vitallium, that cannot be altered or reshaped at the time of surgery without changing the chemical behavior of the material. |
| • PTFE/Carbon-Fiber Prosthesis (FDA Code: KDA / 878.3500) A polytetrafluoroethylene with carbon fibers composite implant material is a porous device material intended to be implanted during surgery of the chin, jaw, nose, or bones or tissue near the eye or ear. The device material serves as a space-occupying substance and is shaped and formed by the surgeon to conform to the patient's need. |