Labanca periosteal elevator #2 handle #6

What is the Labanca #2 elevator handle #6?

The Labanca #2 elevator handle #6 is a specialized manual instrument used in oral surgery for soft tissue management. This device, marketed under the brand Hu-Friedy, consists of a specific Labanca #2 working part mounted on an ergonomic size #6 handle. Its structure is designed to provide a stable grip for practitioners during critical bone exposure phases. As a Class I product, it meets the basic regulatory requirements for reusable surgical instruments. Its design allows for rigorous flap manipulation to access the surgical site with optimal visibility.

What are the clinical indications?

The clinical indications for this instrument from the brand Hu-Friedy primarily concern oral surgery, implantology, and periodontology. It is indicated for periosteal elevation during the creation of full-thickness flaps. Its use is required to expose the alveolar ridge before implant placement or during guided bone regeneration surgeries. The Labanca #2 elevator allows for the gentle separation of soft tissues from the bone without compromising flap integrity. This device is exclusively reserved for healthcare professionals trained in invasive surgical techniques, in accordance with the directives of the manufacturer Hu-friedy located in Chicago, USA.

What are the technical characteristics?

The Labanca #2 elevator is distinguished by its configuration combining a specific working end and a #6 type handle. This handle is designed to ensure precise control of the surgical movement, thereby limiting fatigue during prolonged interventions. Although the exact material composition is not specified in the source data, this instrument from the brand Hu-Friedy belongs to Class I of medical devices. It is manufactured by a recognized manufacturer, Hu-friedy, guaranteeing compliance with industrial manufacturing standards for manual instrumentation. Its technical reference Labanca #2 defines the curvature and width of the spatula to adapt to the anatomy of the oral cavity.

What are the contraindications for use?

According to information provided by the manufacturer Hu-friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. Specific contraindications are not detailed beyond general warnings related to the intended use in a surgical environment. It is the practitioner's responsibility to assess the risks based on the patient's clinical status and the area to be operated on. Use by unqualified personnel constitutes a major contraindication. It is imperative to read the instructions for use carefully before any intervention to become aware of all warnings relating to patient and medical staff safety.

What are the maintenance and handling precautions?

Like any Class I surgical instrument intended for invasive surgery, the Labanca #2 elevator from the brand Hu-Friedy requires a rigorous cleaning and sterilization procedure between each patient. Although resorption details do not apply here as it is a non-implantable instrument, precautions concern the protection of the working parts to maintain their effectiveness. It is recommended to check the integrity of the instrument before each use. Any deformation or abnormal wear of the Labanca #2 tip must lead to the replacement of the device. Compliance with standard decontamination protocols is essential to guarantee aseptic safety during oral surgery procedures.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618, USA. This elevator is classified as a Class I medical device. Compliance with manufacturing standards is ensured by the industrial processes of the manufacturer recognized for its expertise in dental instrumentation. Regulatory information specifies that the product is reserved for healthcare professionals and that the instructions must be consulted before use. Although specific CE marking is not mentioned in the source data, compliance with Class I indicates that the instrument meets the safety and performance requirements defined for this category of manual surgical instruments.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.