Gracey-Curette Turgeon Number 5/6 with handle Number 6 modified - Hu-Friedy - Delynov

What is the Seldin #23 periosteal elevator - Hu-Friedy?

The Seldin #23 periosteal elevator is a specialized manual instrument, manufactured by Hu-Friedy Mfg. Co., LLC, specifically for the field of oral surgery. This Class I medical device is designed to assist the practitioner in soft tissue management. It is distinguished by its structure adapted for the retraction and elevation of mucoperiosteal flaps. As a tool in the Hu-Friedy range, it meets the quality requirements of healthcare professionals for daily surgical procedures, offering a precise interface between the instrumentation and the patient's anatomical structures.

What are the clinical indications for this instrument?

The seldin elevator is primarily indicated for the reflection of the periosteum from the underlying bone tissue. In oral surgery, its use is frequent during the creation of full-thickness flaps. It allows for the clean clearing of the surgical site for procedures such as implant placement, surgical tooth extractions, or guided bone regenerations. The instrument allows for maintaining optimal visibility of the surgical field while preserving the integrity of the soft tissues during their manipulation.

What are the technical characteristics of the Seldin #23 elevator?

The Seldin #23 elevator, referenced under the Hu-Friedy brand, is a robust instrument classified as a Class I medical device. Its design is optimized for grip and control during elevation maneuvers. Although specific materials are not detailed in the provided technical documentation, manufacturing by Hu-Friedy Mfg. Co., LLC guarantees an instrument that complies with professional dental surgery standards. Its specific #23 shape is designed to adapt to various maxillary and mandibular anatomical curvatures.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw MDR text, other than those related to standard surgical protocols. The practitioner must, however, ensure the absence of known allergies to common metallic components of surgical instruments. A prior clinical evaluation of the patient is necessary to validate the feasibility of the surgical procedure involving the use of this elevator.

What are the precautions for use and maintenance?

Like any Class I instrument intended for surgery, the Seldin #23 elevator must be handled with care by trained personnel. The manufacturer Hu-Friedy specifies that it is imperative to read the instructions carefully before use. The instrument must undergo a complete cleaning and sterilization cycle between each patient to prevent risks of cross-contamination. The condition of the instrument should be checked before each procedure to ensure the absence of deformations or damage that could compromise the safety of the surgical gesture.

Who is the manufacturer and what standards are respected?

This device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. It is a Class I medical device, complying with current regulations for manual surgical instruments. The Hu-Friedy brand is recognized in the dental sector for its adherence to rigorous manufacturing protocols. Although CE marking is not specified in the source data, the product meets the safety and performance requirements defined by the manufacturer for professional use in a clinical setting.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.