Mesh Plate 75 x 51 x 0.2mm - Jeil Medical

What is the Jeil Medical 75 x 51 x 0.2mm mesh plate?

The 75 x 51 x 0.2mm mesh plate developed by Jeil Medical is a surgical device used for the reconstruction of bone volumes. It comes in the form of a thin surgical titanium mesh (0.2 mm), offering a balance between rigidity for space maintenance and flexibility for anatomical adaptation. This device acts as a stable physical barrier, allowing the regeneration zone to be delimited while protecting the graft against mechanical pressure from the surrounding soft tissues. Its perforated design facilitates fluid diffusion and vascularization of the surgical site.

What are the clinical indications?

This Jeil Medical device is primarily indicated in guided bone regeneration (GBR) and alveolar reconstruction procedures. Dental surgeons and implantologists use it to treat complex bone defects, whether horizontal or vertical, requiring significant structural support. It is particularly useful during alveolar ridge augmentation before or during implant placement. As a GBR titanium plate, it maintains the volume of the filling material (autograft or bone substitute) throughout the bone healing phase.

What are the technical characteristics?

The technical characteristics of this model include generous dimensions of 75 mm in length by 51 mm in width, allowing it to cover extensive surgical areas or be cut according to the specific needs of the site. The 0.2 mm thickness ensures sufficient thinness to minimize discomfort under mucosal flaps while guaranteeing adequate mechanical strength. Manufactured by Jeil Medical Corp., this plate features a mesh structure that allows for precise handling and stable fixation via osteosynthesis micro-screws not supplied with the device.

What are the contraindications for use?

Contraindications to the use of this mesh plate include clinical situations where an active infection is present at the operative site. Additionally, its use is discouraged in patients with known allergies to the metals constituting the device, although titanium is recognized for its biocompatibility. Uncontrolled systemic pathologies that could compromise bone or mucosal healing, such as unbalanced diabetes or certain metabolic bone diseases, also constitute relative or absolute contraindications to be evaluated by the practitioner before any intervention.

What are the precautions related to its non-resorbable nature?

This mesh plate is a non-resorbable device, meaning it retains its mechanical properties and volume throughout the duration of its implantation. Unlike resorbable membranes, it generally requires a second surgical intervention for its removal once bone consolidation is achieved. The practitioner must ensure hermetic closure of the soft tissues to avoid any early exposure of the surgical titanium mesh, which could lead to bacterial contamination of the graft site. Regular post-operative monitoring is essential to check for the absence of dehiscence.

Who is the manufacturer and what standards are met?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and implantable solutions. Regarding regulatory standards, the risk class and specific CE marking are not mentioned in the current technical data for this CONSO category product. It is the responsibility of the healthcare professional to systematically consult the instructions for use and product labeling provided by Jeil Medical before any implantation to verify the certifications in force and the sterilization or handling protocols recommended by the manufacturer.

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