Lower Left/Upper Right Distal Elevator 5mm - Hu-Friedy Brand - Delynov Online Store

What is the Hu-Friedy 5mm lower left/upper right distal elevator?

The 5mm lower left/upper right distal elevator is a specialized manual instrument designed by the manufacturer Hu-Friedy Mfg. Co., LLC. This surgical device is specifically developed to meet the requirements of practitioners during dental extraction procedures. Its structure is adapted to allow precise and efficient access to distal areas, thus facilitating the luxation of teeth or roots. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation. This 5mm model is intended for rigorous use in clinical settings by qualified healthcare professionals, ensuring handling adapted to oral and implant surgery protocols.

What are the clinical indications for this distal dental elevator?

This distal dental elevator is indicated for oral surgery procedures requiring the elevation or luxation of roots and teeth. It is particularly used in posterior sectors, specifically for the lower left quadrant and the upper right quadrant. Its primary use occurs during the syndesmotomy or initial luxation stage, aiming to break the ligament fibers and mobilize the dental element before its final removal with forceps. The instrument is designed to insert into the periodontal space and apply controlled force. It is suitable for both simple and complex or surgical extractions requiring a precise distal approach to preserve the integrity of the surrounding tissues.

What are the technical characteristics of this Hu-Friedy instrument?

The Hu-Friedy elevator features technical characteristics adapted to the constraints of the oral cavity. With a 5mm working part, it offers an optimal contact surface for the transmission of leverage forces during luxation. The geometry of the instrument is specifically angled to allow reaching the lower left and upper right distal areas without interference with adjacent structures. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the brand's high quality standards. It is categorized as a Class I medical device, which corresponds to reusable non-invasive or invasive surgical instruments for temporary use, requiring rigorous maintenance according to current sterilization protocols.

What are the contraindications for the use of this elevator?

According to information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for duly trained healthcare professionals. Contraindications include the use of the instrument for procedures other than those intended by the manufacturer, or by unqualified personnel. Although the raw MDR text does not list specific biological contraindications such as metal allergies, it is imperative that the practitioner assesses the patient's clinical condition before any intervention. Use on weakened bone structures or in situations where excessive force could lead to a mandibular or tuberosity fracture must be performed with extreme caution, in accordance with good clinical practices in dental surgery.

What are the maintenance precautions for this non-resorbable instrument?

As a reusable metallic surgical instrument and not a resorbable device, this Hu-Friedy elevator requires a strict decontamination and sterilization protocol after each use. The practitioner must carefully read the instructions before use to comply with the cleaning cycles recommended by Hu-Friedy Mfg. Co., LLC. Precautions include regular inspection of the 5mm working part to detect any sign of wear, corrosion, or deformation that could compromise luxation efficiency or patient safety. Storage in a dry and clean environment is essential to maintain the integrity of the Class I instrument between surgical interventions.

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

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is regulatory classified as Class I, in accordance with the safety and performance standards applicable to surgical instruments. Compliance with this classification ensures that the product meets the essential requirements for safe clinical use in dental surgery. As a Class I medical device, it is subject to the declaration of conformity procedures required for its placement on the market. Healthcare professionals must systematically refer to the manufacturer's instructions and the accompanying manual to ensure use in compliance with current regulations.

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Specialized surgical instrumentation is evolving towards ergonomic designs.