Mid Straight Regular Silver t - 0.6 Osteosynthesis Plate with 4 Holes for Dental Surgery by JEIL Medical

What is the Jeil Medical green screw for osteosynthesis plates?

The green screw from Jeil Medical is a fixation component specifically designed for use with a Mid Straight Regular Silver t - 0.6 type osteosynthesis plate featuring 4 holes. This device is part of the Guided Bone Regeneration (GBR) range of solutions offered by the manufacturer Jeil Medical Corp. Its design allows for precise stabilization of plates during bone reconstruction procedures. The green color is a visual indicator facilitating the identification of the component within the Mid Straight osteosynthesis system. This material is intended for practitioners specialized in oral surgery and implantology seeking fixation solutions adapted to grafting and bone stabilization protocols.

What are the clinical indications for this fixation device?

This screw is indicated for the fixation and stabilization of Mid Straight Regular Silver t - 0.6 osteosynthesis plates from the Jeil Medical brand. In oral and maxillofacial surgery, it is used during bone reconstruction procedures, particularly within the framework of Guided Bone Regeneration (GBR). Its role is to ensure the mechanical maintenance of the 4-hole plate against the recipient bone site, thus guaranteeing the immobility necessary for the consolidation of grafts or the protection of the operated area. It is suitable for interventions requiring rigid and reliable fixation to optimize clinical outcomes in implantology.

What are the technical characteristics of the Jeil Medical green screw?

The technical characteristics of this screw are defined by its exclusive compatibility with the Mid Straight Regular Silver t - 0.6 4-hole plate system from Jeil Medical. Although the exact thread dimensions are not specified here, its designation as a 'green screw' allows for rapid recognition during surgical assembly. It is developed by Jeil Medical Corp to integrate perfectly into the threading of the corresponding plates, offering a stable interface. The manufacturing precision of Jeil Medical ensures optimal force transmission during screwing, reducing the risk of mechanical play between the screw and the osteosynthesis plate during the healing phase.

What are the contraindications for the use of this osteosynthesis material?

General contraindications for the use of this fixation device include situations where the bone stock is insufficient to ensure stable anchoring of the screw. Furthermore, use is prohibited in patients with known allergies to the metals or alloys constituting the Jeil Medical osteosynthesis system. Uncontrolled systemic pathologies affecting bone metabolism or healing may also constitute contraindications. It is imperative that the practitioner assesses the quality of the recipient site before the intervention. For an exhaustive list of specific contraindications, one should systematically refer to the instructions for use provided by the manufacturer Jeil Medical Corp.

What precautions should be taken regarding this non-resorbable device?

As a metallic fixation device for osteosynthesis plates, this screw is not resorbable by the body. It is designed to maintain mechanical stability throughout the bone regeneration period. The practitioner must ensure adequate gingival coverage to avoid any exposure of the material, which could compromise the asepsis of the site. Regular postoperative monitoring is necessary to check for the absence of inflammation or mobility of the system. Depending on the established clinical protocol and the progress of bone healing, a second intervention may be scheduled for the removal of the plate and its fixation screws once the regeneration objective is achieved.

Who is the manufacturer and what is the regulatory information?

The device is manufactured by Jeil Medical Corp., a recognized player in the field of medical devices for osteosynthesis and maxillofacial surgery. The Jeil Medical commercial brand guarantees a rigorous manufacturing process. Regarding regulatory aspects such as the risk class, specific CE marking, or exact ISO standards, this information must be verified directly on the product labeling and in the accompanying technical documentation delivered with the material. As a medical device intended for professional use, it must be handled exclusively by qualified dental surgeons or oral surgeons, in accordance with the manufacturer's instructions.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.