Micro Self Tapping Gold OD - 1.3 L - 5 - JEIL Medical

What is the Micro Self Tapping Gold OD - 1.3 L - 5 - JEIL Medical?

The Micro Self Tapping Gold OD is a bone fixation device developed by Jeil Medical for oral and maxillofacial surgery procedures. This 1 3mm titanium screw is distinguished by its specific design intended for guided bone regeneration (GBR). Its structure is optimized to offer immediate primary stability when maintaining filling materials or protective barriers. As a dental micro-surgery screw, it meets the precision requirements of restricted spaces in the alveolar zone. The Gold OD designation refers to its specific finish, while its dimensions (diameter 1.3 mm and length 5 mm) classify it among micro-fixation solutions for demanding practitioners.

What are the clinical indications for this Jeil Medical screw?

This surgery self-tapping screw is primarily indicated in pre-implant bone reconstruction procedures. It is used by dental surgeons and implantologists to securely fix membranes (resorbable or non-resorbable), titanium meshes, or autogenous bone blocks. Its use is common in the treatment of vertical and horizontal bone defects where strict immobilization of the graft or membrane is crucial for the success of osseointegration. Thanks to its reduced diameter, it allows precise application even in complex anatomical sectors or on thin ridges, thus guaranteeing passive tissue maintenance during the healing phase.

What are the technical characteristics of reference 241.011305?

Reference 241.011305 corresponds to a self-tapping titanium screw of 1.3 mm diameter for a length of 5 mm. The major characteristic of this model lies in its self-tapping tip, which allows effective penetration into the bone tissue. This technical specificity reduces mechanical stress during insertion and limits the need for complex drilling instruments for low or medium density bones. Manufactured by Jeil Medical Corp, this screw is designed to be compatible with the instruments of the manufacturer's Micro range. Its 5 mm length offers an ideal compromise for membrane fixation while respecting the integrity of underlying structures.

What are the contraindications for the use of this device?

Contraindications for the use of the Jeil Medical Micro Self Tapping Gold OD screw include clinical situations where bone quality is insufficient to guarantee mechanical stability of the device. Generally, use is prohibited in patients with a known allergy to titanium or its alloys. Uncontrolled systemic pathologies affecting bone metabolism, severely compromised oral hygiene, or active infection at the surgical site also constitute major contraindications. It is the practitioner's responsibility to evaluate risk factors such as heavy smoking or prior irradiation of the jaws before considering the placement of osteosynthesis material.

What are the precautions related to the handling of this non-resorbable screw?

As a titanium device, this screw is non-resorbable and must remain in place for the entire duration necessary for bone consolidation. The practitioner must ensure total and tension-free mucosal coverage to avoid any premature exposure of the material, which could compromise regeneration. During placement, it is recommended to use the specific screwdrivers recommended by Jeil Medical to avoid damaging the screw head or compromising the insertion axis. Once the clinical objective is achieved (usually after several months of healing), the screw can be removed during a second surgical step, often concomitant with implant placement.

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 implantology. As a product distributed by Delynov, this screw meets industrial manufacturing standards for implantable medical devices. Although the specific details of the regulatory class or CE marking are not detailed in this technical sheet, Jeil Medical products are designed according to rigorous quality control processes. Healthcare professionals are invited to systematically refer to the instructions for use and product labeling to verify current certifications and sterilization instructions before any clinical application.

State of the art

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