Mesh Plate 37 x 24 x 0.2mm - Jeil Medical,

What is the 37 x 24 x 0.2mm mesh plate - Jeil Medical?

The 37 x 24 x 0.2mm mesh plate designed by Jeil Medical is a technical device intended for reconstructive and implant surgery. Presented in the form of a titanium mesh plate, it possesses a perforated structure that allows for excellent adaptation to anatomical contours while ensuring a stable physical barrier. With a thickness of 0.2mm, it offers a compromise between thinness to limit soft tissue bulk and rigidity for volume maintenance. This Jeil Medical device is specifically sized to cover intermediate to large bone defects, thus facilitating volume management during grafting.

What are the clinical indications?

This Jeil Medical device is primarily indicated in guided bone regeneration (GBR) protocols and alveolar ridge reconstruction. Dental surgeons and implantologists use it to stabilize bone grafts (autologous or biomaterials) and maintain the necessary space under the mucoperiosteal flap. Its mesh configuration is particularly suitable for horizontal and vertical augmentations where mechanical protection is required to prevent soft tissue collapse into the graft site. It finds its application in cases of severe bone atrophy requiring a rigid support architecture before implant placement.

What are the technical characteristics?

The technical specifications of this Jeil Medical product are based on its precise dimensions of 37mm in length by 24mm in width. The thickness of 0.2mm is a critical parameter that guarantees the malleability necessary for manual modeling or using bending instruments, while maintaining sufficient shape memory to resist indirect masticatory pressures. The mesh design facilitates vascularization of the underlying graft, a key factor for osseointegration and graft survival. The material used, characteristic of Jeil Medical Corp. devices, ensures high biocompatibility essential for prolonged tissue integration without adverse inflammatory reactions.

What are the contraindications for use?

As with any titanium implantable device, contraindications include known allergies to the material or its alloy components. The use of this titanium mesh plate is discouraged in patients with uncontrolled systemic pathologies affecting bone healing or immune metabolism, such as unbalanced diabetes or severe osteoporosis treated with certain bisphosphonates. Insufficient oral hygiene or an active infection at the surgical site also constitute major contraindications. The practitioner must evaluate the benefit-risk ratio in cases of heavy smoking or current or past facial radiotherapy.

What are the precautions related to this non-resorbable device?

This Jeil Medical plate is a non-resorbable device, which means it does not degrade in the body and must generally be removed during a second surgical stage, often at the time of implant placement. Precautions include total coverage by soft tissues to avoid any premature exposure, which could lead to bacterial contamination of the graft site. In case of post-operative mesh exposure, rigorous clinical follow-up is necessary to manage asepsis. Fixation must be ensured by suitable osteosynthesis micro-screws to prevent any micromovement harmful to neo-angiogenesis and bone formation.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Jeil Medical Corp., a recognized player in the field of maxillofacial and dental osteosynthesis. Although specific details regarding the regulatory class or CE marking are not explicitly mentioned in the current technical sheet, Jeil Medical products are developed according to strict industrial manufacturing standards specific to implantable medical devices. It is the practitioner's responsibility to verify the certifications in force on the product labeling and to consult the instructions for use provided by Jeil Medical to ensure the device's compliance with local regulatory requirements before any surgical implantation.

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