Periotome #2, anterior, Black Line

What is the Periotome #2, anterior, Black Line?

The Periotome #2, anterior, Black Line is a precision instrument manufactured by Hu-Friedy, specifically designed for interventions in the anterior sector of the oral cavity. This black periotome is distinguished by its Black Line finish, a characteristic specific to certain instruments of the Hu-Friedy brand. Its structure is optimized to penetrate the narrow space between the tooth root and the alveolar bone. As a Class I medical device, it meets the regulatory requirements for clinical use by qualified practitioners. This tool is essential for dental surgeons seeking to perform fine and controlled movements during the initial phase of dental extractions.

What are the clinical indications?

The use of this dental surgery periotome is indicated during dental extraction procedures, particularly in cases where the preservation of the alveolar bone is critical, such as in immediate implantology. It primarily serves to sever the periodontal ligament (desmodontium) around the entire periphery of the root. By releasing the tooth from its ligamentous attachments before using elevators or forceps, the practitioner reduces the stress exerted on the bone plates. This instrument is specifically adapted for anterior teeth, where aesthetics and vestibular bone volume must be rigorously maintained for the success of future treatments.

What are the technical characteristics?

The Hu-Friedy Periotome #2 features technical characteristics adapted to the constraints of fine oral surgery. Its working part is designed to be both thin and resistant, allowing for atraumatic insertion into the sulcus. The Black Line finish offers improved visual contrast during the procedure, facilitating the identification of anatomical structures in wet or bloody environments. The handle is designed to provide a stable grip, allowing for precise transmission of the axial force necessary to sever the ligament fibers. This device is reusable after following the standard cleaning and sterilization protocols recommended by the manufacturer Hu-Friedy Mfg. Co., LLC.

What are the contraindications for use?

In accordance with the information from the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. General clinical contraindications apply, particularly when the patient's health status does not allow for oral surgical intervention. It is not recommended to use this periotome for excessive leverage functions, as its technical thinness is intended for ligament cutting and not for the forced elevation of massive or ankylosed roots, which could damage the working part. It is imperative to read the instructions carefully before use to respect the intended use by Hu-Friedy Mfg. Co., LLC.

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

As a non-resorbable metallic surgical instrument, the Periotome #2 Black Line requires a rigorous decontamination and sterilization protocol between each patient. Practitioners must ensure that all organic debris is removed immediately after use to prevent corrosion or protein fixation. Although the Black Line finish is robust, it is advisable to use neutral pH cleaning solutions and avoid abrasive agents that could alter the coating of the Hu-Friedy instrument. Regular visual inspection of the working tip is necessary to ensure the absence of micro-cracks or deformations, guaranteeing safety during the surgical act.

Who is the manufacturer and what standards are respected?

The Periotome #2, anterior, Black Line is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This medical device is classified as Class I according to current regulations. As a product from a globally recognized manufacturer in the field of dental instrumentation, it respects the high quality standards imposed by Hu-Friedy. Healthcare professionals must refer to the instructions provided by the manufacturer to guarantee use in compliance with safety standards. Traceability and compliance with Class I regulatory requirements ensure that the instrument is adapted to the requirements of modern oral surgery.

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