Mesh Plate 75x51x0.1mm - Jeil Medical

What is the 75x51x0.1mm mesh plate - Jeil Medical?

The mesh plate developed by Jeil Medical is a support device used in reconstructive surgery. Presented in the form of a fine grid, it has dimensions of 75x51mm with a minimum thickness of 0.1mm. This type of titanium mesh is designed to offer a rigid yet malleable structure, allowing for the maintenance of the space necessary for bone regeneration. Its perforated design is specifically studied to promote fluid exchange and neovascularization within the surgical site. This consumable is integrated into oral surgery protocols where mechanical stabilization of the filling material is required against the pressures exerted by the surrounding soft tissues.

What are the clinical indications for this plate?

This Jeil Medical mesh plate is primarily indicated for the reconstruction of complex alveolar bone defects. It is used by implantologists and oral surgeons during vertical or horizontal guided bone regeneration (GBR) procedures. Its large surface area of 75x51mm allows for the treatment of extensive areas, while its 0.1mm thinness is ideal for minimizing tension during flap closure. It serves as a scaffold to stabilize autologous grafts or bone substitutes, preventing their migration and ensuring the maintenance of the desired volume during the healing phase. It is particularly useful in cases of severe atrophy of the alveolar ridges.

What are the technical characteristics of this device?

The technical specifications of this Jeil Medical Corp. product are based on its precise geometry of 75x51mm. The 0.1mm thickness defines this plate as a fine titanium mesh, offering an optimal compromise between structural strength and clinical flexibility. This thinness allows the practitioner to cut and shape the grid according to the specific anatomy of the patient without creating excessive relief under the gum. The mesh structure ensures dimensional stability while allowing tissue interpenetration. This device is delivered as a technical consumable intended to be fixed, generally by osteosynthesis micro-screws, in order to guarantee total immobilization of the graft-membrane complex during the osseointegration period.

What are the contraindications for the use of this grid?

Although specific data are not listed here, general contraindications for this type of reconstruction grid include known allergies to the constituent metals of the device. Its use is discouraged in patients with uncontrolled systemic pathologies that could compromise bone or mucosal healing, such as severe diabetes or ongoing radiotherapy in the jaw area. Insufficient oral hygiene or an active infection at the surgical site also constitute major contraindications. It is the practitioner's responsibility to evaluate the benefit-risk ratio based on the patient's general health status and the quality of the recipient site before any implantation.

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

The Jeil Medical mesh plate is a non-resorbable device, which means it retains its mechanical properties throughout the healing phase. Particular attention must be paid to soft tissue management to avoid any premature exposure of the grid, which could lead to an infection of the graft site. Flap closure must be achieved without tension. In the majority of clinical cases, this plate must be removed during a second surgical intervention, generally at the time of implant placement, once the bone volume is stabilized. The practitioner must ensure that the cut edges of the mesh are carefully deburred so as not to damage the surrounding tissues.

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. As a product intended for invasive surgery, it is designed according to rigorous manufacturing standards specific to medical devices. Although the exact regulatory class and specific CE marking are not detailed in the present source data, these products are usually subject to international regulations relating to implantable medical devices. To obtain precise details on certifications, applied ISO standards, or sterilization instructions, it is imperative to refer to the instructions for use and labeling provided by Jeil Medical upon delivery of the product.

State of the art

Surgical medical consumables play a decisive role in operative safety.