Micro Self Tapping Gold OD - 1.3 L - 8 - JEIL Medical

What is the Micro Self Tapping Gold OD - 1.3 L - 8 - JEIL Medical?

The Micro Self Tapping Gold OD is a bone fixation device developed by Jeil Medical, specifically intended for oral and implant surgery. This model is distinguished by its self-tapping design, facilitating its insertion into bone structures during reconstruction phases. Identified under reference 241.011308 at Delynov, this micro titanium screw is a key element for practitioners performing guided bone regeneration (GBR) procedures. Its structure is optimized to provide the primary stability necessary to maintain grafting materials or protective barriers.

What are the clinical indications for this micro titanium screw?

This dental micro titanium screw from Jeil Medical is primarily indicated in oral and maxillofacial surgery protocols. It is used for the rigid fixation of bone grafts (onlay or inlay) and the stabilization of non-resorbable or resorbable membranes during GBR procedures. Its use is common in cases of alveolar ridge augmentation where strict immobilization of the regeneration device is imperative for the success of osseointegration. It is suitable for dental surgeons and implantologists seeking a reliable fixation solution for their complex bone reconstructions.

What are the technical characteristics of reference 241.011308?

The Micro Self Tapping Gold screw features precise technical specifications to meet the requirements of micro-osteosynthesis. It has a diameter of 1.3 mm and a length of 8 mm, dimensions adapted to restricted spaces and thin bone volumes in the alveolar zone. Its surgical self-tapping screw function allows for efficient penetration into the bone, reducing operative time by limiting the need for prior manual tapping. Manufactured by Jeil Medical Corp., it is designed to integrate perfectly into the brand's bone surgery kits, guaranteeing optimal compatibility with dedicated pre-drills and screwdrivers.

What are the contraindications for the use of this device?

Contraindications for the use of this micro-osteosynthesis screw include clinical situations where the bone volume is insufficient to ensure stable anchoring of the device. Additionally, use is contraindicated in patients with known allergies to the metals composing the device, although titanium is recognized for its biocompatibility. Uncontrolled systemic pathologies affecting bone metabolism or healing, such as certain severe diabetes or high-dose bisphosphonate treatments, may also constitute relative or absolute contraindications. It is the practitioner's responsibility to evaluate the benefit-risk ratio according to the patient's health status.

What are the precautions related to handling and removal?

As a non-resorbable device, this titanium screw is intended to maintain structures during the bone healing phase. Once graft consolidation or regeneration is achieved, the practitioner must plan its removal during a subsequent surgical phase, generally at the time of implant placement. It is crucial to use the specific gripping and screwing instruments provided by Jeil Medical to avoid any damage to the screw head or neck fracture when applying excessive torque. Rigorous oral hygiene of the patient is essential to prevent any peri-implant inflammation around the fixation site.

Who is the manufacturer and what standards are respected?

The product is manufactured by Jeil Medical Corp., a recognized manufacturer in the field of osteosynthesis and medical devices for cranio-maxillofacial surgery. Although specific details of the regulatory class or CE marking are not mentioned in the source data, Jeil Medical produces its devices according to rigorous quality standards specific to surgical implants. Practitioners are invited to systematically refer to the instructions for use and official labeling provided with the product (reference 241.011308) to verify the current certifications and sterilization protocols recommended by the manufacturer before any intervention.

State of the art

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