Mesh Plate 37 x 25 x 01mm - Jeil Medical

What is the 37 x 25 x 01mm Jeil Medical mesh plate?

The mesh plate developed by Jeil Medical is an implantable device used in oral and maxillofacial surgery. It is a perforated titanium plate with dimensions of 37 x 25 mm and a very thin thickness of 0.1 mm. Its mesh structure allows for excellent diffusion of biological fluids while ensuring a rigid physical barrier. As a 0 1mm titanium mesh, it offers an optimal compromise between mechanical resistance and low bulk under soft tissues, thus facilitating flap closure without excessive tension.

What are the clinical indications for this titanium mesh?

This fine dental titanium mesh is primarily indicated for Guided Bone Regeneration (GBR) procedures. It is used by implantologists and oral surgeons to stabilize bone grafts, whether autologous, allogenic, or synthetic, in horizontal or vertical volume defects. Its function is to maintain the space necessary for osteogenesis by preventing the invagination of epithelial and connective tissues within the graft site. It is particularly useful during reconstructions of atrophied alveolar ridges before or during implant placement.

What are the technical characteristics of this Jeil Medical device?

The technical characteristics of this Jeil Medical product are based on its 37 x 25 mm geometry, adapted to large bone defects. The 0.1 mm thickness makes it a malleable titanium mesh that can be cut and shaped manually by the practitioner to perfectly fit the convexity of the bone ridge. The regular perforation of the mesh promotes vascularization of the graft, a critical factor for the success of bone integration. Its metallic composition ensures high biocompatibility and effective primary stability when fixed with osteosynthesis micro-screws.

What are the contraindications for the use of this plate?

Although specific manufacturer data does not list exhaustive contraindications in this document, standard contraindications for this type of titanium device include known allergies to metals or alloy components. Use is discouraged in patients with uncontrolled systemic pathologies affecting bone healing or in cases of active infections at the surgical site. It is the surgeon's responsibility to evaluate the benefit-risk ratio based on the patient's general health status, particularly in cases of heavy smoking or prior jaw irradiation.

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

The Jeil Medical mesh plate is a non-resorbable device, which means a second surgical intervention is necessary for its removal after bone consolidation, generally after a period of 4 to 9 months depending on the clinical case. Particular attention must be paid to the total coverage of the plate by soft tissues to avoid any premature exposure, which could compromise the graft. The practitioner must take care to carefully deburr the edges after cutting the fine dental titanium mesh to prevent any irritation or perforation of the gingival mucosa.

Who is the manufacturer and what standards are respected?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and implantology. Although the regulatory class and specific CE marking are not detailed in the current technical sheet, Jeil Medical products are designed according to rigorous industrial manufacturing protocols specific to implantable medical devices. For any precise information regarding regulatory compliance, ISO certifications, or detailed instructions for use, it is imperative to refer to the technical notice provided by Jeil Medical with the product or to contact support services.

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