Smooth horizontal flexion plate for implantology, oral surgery and maxillofacial surgery - Jeil Medical (12-GM-L01) - Delynov

What is the Jeil Medical horizontal bending plate?

The smooth horizontal bending plate, referenced under code 12-GM-L01, is an osteosynthesis device designed by Jeil Medical Corp. This component is specifically developed to meet the requirements of oral and maxillofacial surgery. Its structure is distinguished by a smooth surface and a horizontal bending capacity, allowing the practitioner to adjust it according to the specific morphology of the surgical site. As a maxillofacial bending plate, it ensures the maintenance of bone structures while minimizing submucosal bulk thanks to its optimized profile. This device is a key element for interventions requiring rigid yet adaptable stabilization.

What are the clinical indications for this device?

This maxillofacial osteosynthesis plate is indicated for a wide range of procedures in oral and implant surgery. It is primarily used for the internal fixation of fractures, the stabilization of osteotomies, and the maintenance of bone grafts during complex reconstructions. Its horizontal bending capacity makes it particularly useful in areas where the bone anatomy presents specific curvatures requiring precise plating. Surgeons also use it in maxillofacial surgery protocols to ensure the durability of the anchorage and the primary stability essential for complication-free bone healing.

What are the technical characteristics of the 12-GM-L01 plate?

The smooth horizontal bending plate is characterized by its technical reference 12-GM-L01, guaranteeing rigorous traceability within the Jeil Medical range. Its smooth design is engineered to reduce potential irritation of the surrounding soft tissues after placement. The horizontal bending specificity allows for controlled deformation of the device to follow bone contours without compromising the mechanical strength of the assembly. Although exact dimensions are not specified here, this type of oral surgery titanium plate is recognized for its optimal ratio between thinness and stability, offering a reliable solution for maintaining bone segments in an anatomical position.

What are the contraindications for using this plate?

Contraindications for the use of this osteosynthesis plate generally include clinical situations where the bone stock is insufficient to guarantee stable anchorage of the fixation screws. Similarly, any known allergy or hypersensitivity to the metals constituting the device (often titanium alloys in maxillofacial surgery) constitutes an absolute contraindication. Active infections at the surgical site or serious systemic disorders compromising vascularization and bone healing must be carefully evaluated by the surgeon. It is imperative to refer to the technical instructions from the manufacturer Jeil Medical Corp. for the exhaustive list of contraindications related to the material and design.

What precautions should be taken for a non-resorbable device?

As it is a metallic fixation device, this surgical bending plate is non-resorbable. It is intended to remain in place throughout the bone consolidation phase. The practitioner must ensure total and tension-free mucosal coverage to avoid any postoperative exposure of the material. Particular attention must be paid during shaping not to create areas of weakness through excessive or repeated bending. Depending on the clinical protocol and the progress of healing, a second intervention may be scheduled for the removal of the osteosynthesis material once bone fusion is complete and stabilized, in accordance with oral surgery standards.

Who is the manufacturer and what standards are met?

The device is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of instrumentation and implants for maxillofacial surgery. The product is distributed by Delynov under the commercial name Jeil Medical. Regarding regulatory certifications such as the device class or specific CE marking, this information is not detailed in the current technical documentation. It is the responsibility of the healthcare professional to verify the device's compliance with local requirements and to consult the labeling as well as the user manual provided by Jeil Medical to confirm the approvals in effect at the time of use.

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