Mesh Plate 99 x 74 x 0.1mm - Jeil Medical

What is the 99 x 74 x 0.1mm mesh plate - Jeil Medical?

The mesh plate developed by Jeil Medical is a device intended for reconstructive and implant surgery. Presented in the form of a large-sized gbr titanium mesh (99 x 74 mm), it is distinguished by an extremely thin thickness of 0.1mm. This mesh structure is specifically designed to provide mechanical support during bone grafts while allowing optimal diffusion of biological fluids. This device from Jeil Medical Corp. is used by practitioners to secure bone substitutes and promote the formation of new mineralized tissue under the gingiva.

What are the clinical indications for this surgery titanium mesh?

This surgery titanium mesh is primarily indicated in guided bone regeneration (GBR) protocols for the treatment of maxillary and mandibular bone defects. It is used to maintain the space necessary for bone growth, preventing soft tissue invasion into the graft site. Its application is common during horizontal or vertical ridge augmentations prior to implant placement. Thanks to its generous dimensions, it can be cut to adapt to surgical sites of various sizes, offering significant flexibility during complex alveolar reconstruction interventions.

What are the technical characteristics of this Jeil Medical device?

The Jeil Medical mesh plate features precise technical specifications to meet the requirements of oral surgery. It measures 99 mm in length by 74 mm in width, thus covering extensive surfaces. Its 0.1mm thickness ensures optimal malleability, allowing the surgeon to conform it precisely to the patient's anatomy without creating excessive volume under the mucosal flaps. As a dental titanium plate, it possesses the intrinsic biocompatibility properties associated with its material, guaranteeing stable tissue integration throughout the bone healing phase.

What are the contraindications for the use of this dental titanium plate?

The use of this dental titanium plate is contraindicated in patients with a known hypersensitivity or allergy to metals, and specifically to titanium. Generally, in the absence of specific data in the reference text, standard contraindications in oral surgery apply: active infections at the surgical site, uncontrolled systemic pathologies affecting healing (such as severe diabetes or untreated osteoporosis), or insufficient oral hygiene. It is the practitioner's responsibility to evaluate the benefit-risk ratio for each patient before implanting this non-resorbable device.

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

As a non-resorbable type osteosynthese titanium plate, this device requires a second surgical intervention for its removal once bone consolidation is achieved. The main precautions concern mesh exposure: a hermetic and tension-free closure of the soft tissues is crucial to avoid post-operative complications. In case of early exposure, a rigorous decontamination protocol must be implemented. The practitioner must ensure that the edges of the mesh, after cutting, are carefully deburred so as not to damage surrounding tissues or cause flap perforation.

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 implantable solutions. Although the specific regulatory class and CE marking are not detailed in the technical documentation provided, Jeil Medical products are designed according to rigorous quality standards specific to implantable medical devices. To obtain precise information on current certifications, the risk class (generally Class IIb for permanent implants) or sterilization instructions, it is imperative to refer to the instructions for use and the official labeling accompanying the product.

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