Elevator number 38 with handle number 510 left striated - Hu-Friedy - Delynov

What is the Hu-Friedy #38 elevator #510 left serrated handle?

The #38 elevator #510 left serrated handle is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is specifically designed for oral surgery interventions requiring effective luxation of roots or teeth. Its structure consists of a left-oriented working part and a #510 type handle, characterized by a serrated surface. This design allows the practitioner to maintain a firm and stable grip, limiting the risk of slipping when applying rotational or leverage forces. As an instrument in the INSTRU category, it meets the quality requirements of a recognized manufacturer in the field of surgical instrumentation.

What are the clinical indications?

This left dental elevator is indicated for exodontia procedures, including the luxation of teeth prior to the use of forceps or the extraction of fractured roots. Its use is particularly relevant in restricted access areas where a left lateral orientation is necessary to apply effective leverage against the alveolar bone. It helps separate the periodontal ligament from the root structure, thus facilitating avulsion while preserving the integrity of the surrounding bone plates, which is crucial in pre-implant alveolar preservation protocols. This device is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of this instrument?

The instrument is distinguished by the combination of the #38 tip design and the ergonomics of the #510 handle. The active part is oriented for specific left-side use, allowing precise insertion into the periodontal space. The serrated #510 handle offers a texture that improves handling safety, even in wet environments. This medical device belongs to Class I according to current regulations. Manufacturing by Hu-Friedy guarantees a robust design adapted to repeated mechanical stresses during luxation maneuvers. Every detail, from the handle serration to the tip curvature, is designed to transmit force in a controlled manner to the surgical site.

What are the contraindications for use?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the intended use. However, the use of this instrument is contraindicated for any unqualified personnel, as it is exclusively reserved for healthcare professionals. It must not be used outside of its intended application of dental luxation. The practitioner must assess the condition of the alveolar bone and root fragility before any application of excessive force to avoid complications such as tuberosity fractures or sinus projections, in accordance with good clinical practices in dental surgery.

What are the maintenance and use precautions?

Like any Class I instrument intended for surgery, this elevator must be handled with care. Before the first use and after each intervention, it is imperative to follow the cleaning, disinfection, and sterilization protocols in force in dental practices. It is strongly advised to read the instructions carefully before use to comply with the recommendations of the manufacturer Hu-Friedy. Checking the condition of the tip and the serrated handle before each procedure is necessary to guarantee patient safety and the effectiveness of the surgical movement. Particular attention must be paid to the removal of any organic residue in the handle serrations during the cleaning cycle.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device. Hu-Friedy is a manufacturer recognized for its compliance with rigorous manufacturing standards, ensuring the reliability of surgical instruments provided to odontologists and oral surgeons worldwide. Although specific CE marking is not mentioned in the source data, the instrument complies with the regulatory requirements applicable to devices of its class for professional marketing. Practitioners should refer to the instructions provided by the company to ensure use in accordance with safety standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.