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

What is the Jeil Medical micro-screw and Mesh plate block (112-060)?

The micro-screw and Mesh plate block from the Jeil Medical brand, bearing reference 112-060, is a specialized device designed for Guided Bone Regeneration (GBR) procedures. This system is specifically developed by Jeil Medical Corp. to meet the needs of dental surgeons and implantologists during complex bone reconstructions. The set combines micro-screws and a mesh structure allowing for optimal stabilization of bone grafts. This Delynov product stands out for its rigorous technical design, aiming to offer a reliable solution for maintaining the space necessary for bone neoformation while ensuring precise fixation of the components.

What are the clinical indications for this Jeil Medical device?

This Jeil Medical device is primarily indicated for oral surgery, maxillofacial surgery, and implantology. It is used during Guided Bone Regeneration (GBR) protocols to stabilize filling materials or membranes. Its use is recommended for the treatment of alveolar bone defects, allowing for the maintenance of the architecture necessary for future implant placement. As a fixation tool, it ensures the immobilization of the mesh and grafts, a critical step for the success of bone integration. Practitioners use this block for ridge augmentations or bone volume reconstructions where high mechanical stability is required.

What are the technical characteristics of reference 112-060?

Reference 112-060 from Jeil Medical corresponds to a technical block including micro-screws and a mesh plate. Although specific dimensions and detailed materials are not explicitly mentioned in the raw technical sheet, this type of device is recognized for its thinness and structural strength. The design of the mesh allows for easy handling to adapt to the specific anatomy of the surgical site. The associated micro-screw system is designed for precise insertion, guaranteeing solid anchorage in the surrounding bone tissue. This complete kit allows for simplified management of instrumentation during the operative phases of fixation in implant surgery.

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

The use of the Jeil Medical micro-screw and Mesh plate block must be evaluated by the practitioner based on the patient's clinical condition. General contraindications include uncontrolled systemic pathologies affecting bone healing, such as unbalanced diabetes or severe osteoporosis. Active local infections at the surgical site or insufficient oral hygiene also constitute major contraindications. It is imperative to check for the absence of known hypersensitivity to the metallic components of the device. Surgeons must systematically consult the instructions for use provided by Jeil Medical Corp. to ensure the compatibility of the device with each patient's specific health profile.

What are the precautions for use for this non-resorbable device?

This type of fixation and maintenance device (mesh and screws) is generally non-resorbable, meaning it maintains its structural integrity throughout the bone healing phase. Particular attention must be paid to soft tissue coverage to avoid any exposure of the mesh, which could compromise regeneration. The practitioner must ensure rigorous sterile handling and tension-free fixation of the flaps. A second surgical intervention is generally necessary to remove the hardware once the desired bone volume has stabilized. Post-operative follow-up is crucial to detect any signs of inflammation or early dehiscence.

Who is the manufacturer and what standards are respected by this product?

The device is manufactured by Jeil Medical Corp., a major player in the field of surgical fixation solutions. Although specific information regarding the regulatory class, CE marking, or ISO certifications is not detailed in the current source data, Jeil Medical is recognized for its production standards in oral surgery. Healthcare professionals are invited to refer to the product labeling and the official technical documentation delivered with reference 112-060 to confirm the certifications in force. Delynov ensures the provision of devices from specialized manufacturers that respect the rigorous manufacturing protocols specific to implantable medical devices.

State of the art

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