Labanca periosteal elevator #6 handle - Hu-Friedy - Delynov

What is the Hu-Friedy Labanca handle #6 elevator?

The Labanca handle #6 elevator, designed by the manufacturer Hu-Friedy, is a specialized manual instrument used in oral surgery. This device is distinguished by its robust structure and its #6 type handle, offering ergonomics adapted to prolonged interventions. As a high-quality dental elevator, it is intended for the manipulation of soft tissues and the exposure of bone structures. Hu-Friedy Mfg. Co., LLC ensures the manufacturing of this instrument according to rigorous standards, guaranteeing constant reliability for practitioners. This model is specifically developed to meet the needs of dental surgeons and implantologists during operative site preparation.

What are the clinical indications for the Labanca elevator?

The Labanca oral surgery elevator is primarily indicated for the elevation of the mucoperiosteal flap. Its use is essential during implant placement surgeries, guided bone regenerations, or corrective periodontal surgeries. The instrument allows for the precise separation of the periosteum from the alveolar bone, thus providing optimal visibility of the surgical field. It is also used to retract tissues without excessive laceration, thereby facilitating post-operative healing. This Hu-Friedy device is exclusively reserved for healthcare professionals trained in oral surgery techniques, in accordance with the instructions for use from the manufacturer located in Chicago.

What are the technical characteristics of this instrument?

The Hu-Friedy Labanca elevator is characterized by its number 6 handle, a specific diameter that improves tactile control during moderate force maneuvers. The design of the working end is engineered to effectively insert into the subperiosteal space. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument benefits from a meticulous finish allowing for cleaning and sterilization in compliance with hospital and office protocols. Although the exact composition is not specified in the source data, the reputation of the manufacturer Hu-Friedy is based on the use of materials suitable for Class I surgical instrumentation, ensuring the mechanical resistance necessary for the stresses of tissue elevation.

What are the contraindications for the use of this elevator?

According to the information provided by Hu-Friedy, specific contraindications are not listed exhaustively beyond general warnings. However, the use of this instrument is strictly reserved for qualified healthcare professionals. Inappropriate use by untrained personnel constitutes a major contraindication, which could lead to tissue or bone damage. One should systematically refer to the instructions for use provided by the manufacturer Hu-Friedy Mfg. Co., LLC before any intervention. Practitioners must also evaluate the patient's tissue condition to ensure that the instrumentation is adapted to the morphology and the pathology being treated.

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

As it is a metallic surgical instrument and not an absorbable device, the Hu-Friedy Labanca elevator requires a rigorous decontamination and sterilization protocol after each use. It is imperative to follow the cleaning instructions recommended by Hu-Friedy to maintain the integrity of the instrument and prevent risks of cross-contamination. Precautions include regular visual inspection to detect any wear or deformation of the active tip. Inadequate maintenance could compromise the precision of the elevation or the durability of the device. Careful reading of the instructions for use is essential to guarantee the safety of the patient and the practitioner during each oral surgery procedure.

Who is the manufacturer and what standards are respected?

The Labanca elevator is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, IL 60618, USA. This medical device is listed as Class I, which corresponds to reusable surgical instruments presenting a low risk to the patient. Although the specific CE marking is not mentioned in the source data, the instrument complies with the regulatory requirements applicable to devices of its class. As a Hu-Friedy product, it is subject to the manufacturer's strict quality controls. It is reminded that this instrument is exclusively reserved for professional use and that it is necessary to read the instructions carefully before any clinical implementation.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.