Elevator Seldin Number 4L Left Maxillary Molar Short - Hu-Friedy - Delynov

What is the Seldin #4L M #510 elevator?

The Seldin #4L M #510 elevator, manufactured by Hu-Friedy, is a manual surgical instrument used in dentistry and oral surgery. It belongs to the category of consumables and precision instruments intended for dental luxation. This specific model, referenced under the designation 4L, features a configuration oriented to facilitate access to difficult areas. As a product of Hu-Friedy Mfg. Co., LLC, this instrument meets the manufacturing requirements of a recognized manufacturer in the global dental sector. Its structure is designed to transmit the forces necessary for elevation without compromising the integrity of the surrounding tissues when used by a qualified professional.

What are the clinical indications?

This instrument is primarily indicated for simple or complex tooth extraction procedures. Its main role is to act as a left molar elevator to mobilize teeth or residual roots before final extraction. It is particularly useful for breaking the periodontal ligament fibers and widening the socket, thus facilitating the passage of forceps. The use of this left Seldin elevator is recommended in cases where access to the left mandibular or maxillary molars requires a specific angulation. It allows for a controlled leverage application, essential when managing impacted teeth or fractured roots in oral and implant surgery.

What are the technical characteristics?

The Seldin #4L M #510 elevator is distinguished by its morphology adapted to molar sectors. The 4L designation indicates a specific orientation for the left side, optimizing ergonomics during the intervention. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument is classified as a Class I medical device. Its short design allows for precise handling in the restricted spaces of the oral cavity. Although specific materials are not detailed in the provided technical documentation, Hu-Friedy's manufacturing standards ensure resistance adapted to the mechanical stresses encountered during dental luxation. The instrument must be used in accordance with the instructions from the manufacturer located in Chicago, USA.

What are the contraindications for use?

The contraindications associated with the use of this instrument are those generally observed in oral surgery for this class of devices. According to information from the manufacturer Hu-Friedy, use is strictly reserved for qualified healthcare professionals. It must not be used outside of its intended use, namely dental luxation and elevation. Contraindications may include clinical situations where bone integrity is too fragile to support a leverage effect or when the patient presents systemic pathologies contraindicating any invasive surgery. It is imperative to read the instructions carefully before use to identify any specific restrictions related to the clinical protocol or the patient's health status.

What are the maintenance and durability precautions?

As a non-resorbable Class I instrument, precautions for use rely on rigorous handling by the practitioner. Although sterilization details are not specified in the source data, this type of Hu-Friedy instrument is intended for repeated professional use requiring appropriate cleaning and disinfection between each patient. The practitioner must ensure not to exert excessive force that could damage the tip or handle of the elevator. The durability of the instrument depends on compliance with the maintenance cycles recommended by Hu-Friedy 3232 N. Rockwell St. Chicago, Il 60618 USA. A visual inspection before each intervention is recommended to ensure the absence of deformation or premature wear.

Who is the manufacturer and what standards are respected?

The Seldin #4L M #510 elevator is manufactured by Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a product from a manufacturer recognized for its expertise in dental instrumentation, it meets the quality standards required for medical devices reserved for healthcare professionals. Although specific CE marking is not mentioned in the source data, compliance with Class I directives ensures that the product is designed for safe clinical use. Practitioners should refer to the enclosed instructions for any additional information regarding warnings and implementation of the device.

State of the art

Surgical medical consumables play a decisive role in operative safety.