Micron Screw Block and Mesh Plate - Jeil Medical (112-060) - Delynov

What is the Jeil Medical micro-screw and Mesh plate block?

The micro-screw and Mesh plate block, referenced under code 112-060, is a surgical device designed by Jeil Medical. This product is specifically developed for Guided Bone Regeneration (GBR) procedures. It consists of a structured assembly including micro-screws and a mesh plate, providing practitioners with a fixation and maintenance system for bone grafts or membranes. The design by Jeil Medical Corp. ensures precise integration within the dedicated instrumentation for oral and implant surgery, thereby facilitating the stabilization of bone volumes during reconstruction phases.

What are the clinical indications for this device?

The Jeil Medical 112-060 block is primarily indicated in oral, maxillofacial, and implant surgery protocols requiring Guided Bone Regeneration (GBR). It is used for the rigid fixation of bone fragments or the maintenance of reinforcement structures (mesh) during the filling of alveolar bone defects. This device helps maintain the space necessary for bone neoformation while protecting the surgical site from the mechanical stresses of the surrounding soft tissues. Its use is reserved for dental surgeons and stomatologists trained in complex bone reconstruction techniques.

What are the technical characteristics of the 112-060 block?

The Jeil Medical micro-screw and Mesh plate block is characterized by its technical reference 112-060. It is designed to offer optimal compatibility between the fixation elements (micro-screws) and the support structure (mesh plate). Although specific dimensions are not detailed here, the Jeil Medical range is recognized for its machining precision, allowing for easy handling during placement. This system is developed to meet the primary stability requirements essential in implantology, ensuring that the device remains in place throughout the bone healing period.

What are the contraindications for the use of this GBR material?

The use of the Jeil Medical micro-screw and Mesh plate block is contraindicated in patients with uncontrolled systemic pathologies that could compromise bone healing or increase the risk of infection. Contraindications also include known allergies to the metallic components of the device, surgical sites with active infection, or insufficient vascularization. It is the practitioner's responsibility to assess the benefit/risk ratio based on the patient's general health status, oral hygiene, and medical history before any bone regeneration intervention.

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

As a metallic fixation device composed of micro-screws and a mesh plate, this material is by nature non-resorbable. Particular attention must be paid to the hermetic closure of soft tissues to avoid any post-operative exposure of the device, which could lead to infection or graft failure. The practitioner must plan a second surgical intervention for the removal of the material once bone consolidation is deemed satisfactory. Rigorous post-operative follow-up is essential to monitor the stability of the Jeil Medical block and the absence of inflammatory complications.

Who is the manufacturer and what standards are respected?

This device is manufactured by Jeil Medical Corp., a specialist in the design of osteosynthesis and bone regeneration solutions. The product is marketed under the Jeil Medical brand. In accordance with safety requirements for medical devices, the manufacturer ensures the traceability and production quality of its micro-screw and plate systems. For any specific information regarding the regulatory class, CE marking, or certifications specific to reference 112-060, it is imperative to refer to the instructions for use and technical documents provided by the manufacturer at the time of purchase.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.