Luxator 4mm Straight Black Series Elevator - Hu-Friedy - Delynov

What is the Hu-Friedy Black Line 4mm straight luxating instrument?

The Black Line 4mm straight luxating instrument is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is distinguished by its specific 'Black Line' finish and its straight tip with a width of 4mm. Unlike a standard elevator, this 4mm dental luxating instrument is designed with a thin, sharp blade to penetrate the periodontal space. Its structure is optimized for the sectioning of periodontal ligaments, allowing for a rigorous surgical approach. As a product of the Hu-Friedy range, it meets the quality requirements of practitioners performing simple or complex extractions in oral surgery.

What are the clinical indications for this 4mm luxating instrument?

The use of the 4mm straight luxating instrument is primarily indicated during tooth avulsion procedures. It is used by dental surgeons and implantologists to perform syndesmotomy and the initial luxation of the tooth or root. By inserting the 4mm tip into the periodontal space, the practitioner can effectively section the supporting fibers. This clinical maneuver is crucial for reducing bone resistance before using forceps. The instrument is particularly suited for areas where straight access is possible, facilitating the preservation of the integrity of the alveolar bone plate, a fundamental aspect in pre-implant surgery.

What are the technical characteristics of this instrument?

The 4mm straight luxating instrument benefits from Hu-Friedy manufacturing expertise. Its main characteristic lies in its 4mm wide straight blade, designed to offer an ideal compromise between penetration thinness and mechanical resistance. The Black Line series incorporates a dark coating that improves visual contrast at the operative site while optimizing the glide of the instrument. This device is classified as a Class I instrument according to current regulations. Its ergonomic design allows for controlled transmission of axial force during insertion into the ligament, ensuring precise handling by the healthcare professional.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this luxating instrument is strictly reserved for qualified healthcare professionals. Contraindications include using the instrument for tasks for which it is not intended, such as elevating dense bone structures with excessive leverage, which could damage the thin 4mm blade. One should systematically refer to the instructions for use and follow sterilization protocols. Any local or systemic pathology contraindicating invasive oral surgery constitutes, by extension, a contraindication to the use of this luxation instrument.

What are the precautions for use and maintenance for this luxating instrument?

Like any Class I instrument intended for surgery, the Hu-Friedy 4mm straight luxating instrument requires rigorous maintenance. It is imperative to read the instructions carefully before the first use. The instrument must be cleaned, disinfected, and sterilized according to the cycles validated by the manufacturer to ensure patient safety and the longevity of the Black Line finish. The practitioner must inspect the condition of the 4mm tip before each intervention to ensure the absence of deformations or dullness. Careful handling is required to avoid any excessive lateral stress that could compromise the structural integrity of the thin blade.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This 4mm dental luxating instrument complies with the regulations for Class I medical devices. Hu-Friedy is globally recognized for its high production standards in the field of surgical instrumentation. Compliance with manufacturing protocols ensures healthcare professionals a reliable tool for their daily practice. As a Class I medical device, it meets the essential safety and performance requirements defined for this category of non-invasive or short-term invasive manual and rotary instruments.

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