Mesh Plate 49 x 37 x 0.1mm - Jeil Medical

What is the 49 x 37 x 0.1mm mesh plate - Jeil Medical?

The Jeil Medical mesh plate is a technical device used in oral and maxillofacial surgery. Presented in the form of a dental titanium grid, it has dimensions of 49 mm in length by 37 mm in width with an extremely thin thickness of 0.1 mm. This specific structure allows the practitioner to benefit from a malleable support capable of adapting to complex bone reliefs. This device is designed by Jeil Medical Corp., a manufacturer recognized for its osteosynthesis solutions, to meet the mechanical maintenance requirements during reconstruction phases.

What are the clinical indications for this device?

This type of mesh plate is mainly indicated in alveolar ridge reconstruction protocols and pre-implant bone augmentations. As a GBR (Guided Bone Regeneration) titanium mesh, it serves as a physical barrier to maintain bone substitutes or autologous bone in place, preventing the invasion of connective tissues into the bone defect. Its use is common for stabilizing volume in areas with significant substance loss where a simple membrane would not suffice to ensure the necessary structural rigidity during the healing phase.

What are the technical characteristics of this plate?

The Jeil Medical mesh plate is distinguished by its thickness of 0.1 mm, which gives it the properties of a malleable titanium plate. This reduced thickness facilitates manual cutting and shaping by the surgeon to precisely fit the area to be treated. Its perforated surface (mesh) promotes fluid diffusion and vascularization of the underlying graft, which are critical factors for successful bone integration. The 49 x 37 mm dimensions offer a generous working surface, suitable for medium to large-sized defects in oral surgery.

What are the contraindications for the use of this mesh plate?

Contraindications mainly include known hypersensitivities or allergies to the metallic components of the device. Additionally, use is discouraged in sites with an active untreated infection or insufficient local vascularization that would compromise healing. As with any fixation device, adequate soft tissue coverage is necessary to avoid plate exposure. Patients suffering from severe bone metabolic disorders or uncontrolled systemic pathologies may present relative contraindications to the surgical procedure itself.

What are the precautions related to handling and non-resorption?

This device is non-resorbable, meaning it retains its mechanical properties and volume throughout the bone consolidation phase. Particular attention must be paid to the fixation of the plate to avoid any micro-movement, often using adapted osteosynthesis micro-screws. The practitioner must ensure that any sharp edges are eliminated after cutting the mesh to prevent mucosal perforations. A second surgical intervention is generally scheduled after several months to remove the plate once the bone volume is stabilized and ready for implantation.

Who is the manufacturer and what standards are respected?

The product is manufactured by Jeil Medical Corp., a company specializing in the design of high-precision medical devices for cranio-maxillofacial and dental surgery. Regarding specific regulatory standards and certifications, such as the risk class or CE marking, it is imperative to systematically refer to the product labeling and the instructions for use provided by Jeil Medical. The practitioner must verify the compliance of the device with current local regulations before any clinical implantation.

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