6 anterior Handle Allen Key - Hu-Friedy - Delynov

What is the Allen elevator periosteal anterior #6 handle?

The Allen elevator periosteal anterior #6 handle is a specialized manual instrument developed by the manufacturer Hu-Friedy Mfg. Co., LLC. It belongs to the surgical instruments category (INSTRU) and is distinguished by its configuration optimized for the anterior sector. This allen elevator instrument is structured with a #6 type handle, offering a specific working interface for demanding practitioners. As a Class I medical device, it meets the rigorous manufacturing standards of Hu-Friedy, guaranteeing reliable integration into oral surgery protocols. Its design primarily targets the manipulation of soft tissues and the periosteum with the technical rigor characteristic of this recognized brand's instruments.

What are the clinical indications for this instrument?

This periosteal elevator instrument is indicated for oral, periodontal, and implant surgery procedures requiring direct visual and instrumental access to the alveolar bone. The allen elevator is specifically used for full-thickness flap elevation, allowing for the controlled detachment of the periosteum from the bone. Its use is particularly relevant in the anterior sector to prepare the site before implant placement, guided bone regeneration, or during muco-gingival surgeries. According to Hu-Friedy guidelines, the use of this device is strictly reserved for qualified healthcare professionals mastering tissue detachment techniques.

What are the technical characteristics of this elevator?

The Allen elevator periosteal is characterized by its number 6 handle, an ergonomic specificity of the Hu-Friedy range facilitating control during critical detachment phases. Although exact composition details are not specified, manufacturing by Hu-Friedy Mfg. Co., LLC ensures a finish quality compliant with Class I requirements. This periosteal elevator is designed to offer a precise tactile response during the separation of connective fibers. Its morphology is adapted to the anatomy of the anterior zone, allowing effective insertion under the gingival margin and fluid progression along the bone cortex without compromising the integrity of adjacent tissues.

What are the contraindications for the use of this device?

In accordance with information provided by the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively beyond standard safety warnings. However, the use of this instrument is formally reserved for healthcare professionals. Its use is contraindicated for any person not possessing adequate surgical training. It is also necessary to respect the sterilization and maintenance protocols recommended by Hu-Friedy to avoid any risk of cross-contamination or instrument failure. The practitioner must refer to the instructions for use before any intervention to validate the suitability of the instrument with the patient's clinical status.

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

As it is a reusable metallic surgical instrument and not a resorbable device, the longevity of the allen elevator depends on the rigor of the cleaning and sterilization cycles. Hu-Friedy recommends a careful reading of the instructions for the processing of its Class I instruments. Precautions include the use of appropriate cleaning agents that do not alter the properties of the instrument. It is essential to check the integrity of the active tips of the periosteal elevator instrument after each cycle to ensure the absence of corrosion or deformation. Careful handling during decontamination prevents premature wear and guarantees patient safety during subsequent interventions.

Who is the manufacturer and what standards are respected?

The Allen elevator periosteal is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for its compliance with quality standards in the production of surgical instrumentation. Each instrument is subject to strict controls to meet the requirements of healthcare professionals. Although specific CE marking is not mentioned in the source data, the Class I status indicates compliance with essential safety and performance requirements for medical devices distributed by Delynov.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.