Periotome number 5 anterior Black series angled Hu-Friedy Delynov

What is the Hu-Friedy #5 Black Line periotome?

The #5 Black Line periotome is a precision instrument manufactured by Hu-Friedy, specifically designed for oral surgery procedures. This model is distinguished by its angled configuration and its Black Line finish, a surface technology unique to the manufacturer Hu-Friedy Mfg. Co., LLC. Unlike classic syndesmotomes, this instrument has a thin blade intended to be inserted deeply into the ligament space. Its structure is optimized for the anterior sector, allowing the practitioner to operate with great finesse. As a Class I medical device, it meets the quality requirements necessary for daily surgical procedures in dental offices or hospital environments.

What are the clinical indications for this angled periotome?

The use of this angled periotome is primarily indicated during atraumatic tooth extractions, particularly in the context of pre-implant surgeries. Its role is to sever the fibers of the periodontal ligament (desmodontium) around the entire circumference of the root. By releasing the tooth from its ligamentous attachments without exerting excessive lateral pressure, it allows the alveolar bone to remain intact, which is crucial for the success of a future implant placement. It is particularly effective in the anterior sector where the thinness of the vestibular bone plates requires extremely delicate manipulation to avoid any post-operative fracture or resorption.

What are the technical characteristics of this instrument?

The #5 Black Line periotome features specific technical characteristics developed by Hu-Friedy. Its working part is angled, which offers an ideal angle of attack for anterior sites, facilitating penetration into the sulcus. The Black Line range is characterized by a dark coating that reduces reflections under operating lights, thus improving visibility of the surgical field. The thinness of the blade is calibrated to penetrate the narrow space between the root and the alveolar bone without damaging the surrounding soft tissues. This instrument is designed to be sterilizable and reusable, in accordance with strict oral surgery hygiene protocols.

What are the contraindications for the use of this device?

According to information from the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed other than those related to classic tooth extraction procedures. However, it is imperative not to use this instrument as a lever or an elevator. Its thin blade is not designed to withstand significant torsional forces or lifting pressures, which could lead to a fracture of the working tip. The practitioner must ensure the absence of underlying pathologies prohibiting the surgical act itself before any intervention.

What are the precautions for use and maintenance?

Like any Class I instrument intended for surgery, the #5 periotome must be handled with care. Before the first use and after each procedure, it must be cleaned, disinfected, and sterilized according to the instructions provided by Hu-Friedy. It is essential to read the instructions carefully before use. The practitioner must inspect the instrument to verify the integrity of the blade and the Black Line coating. Inappropriate use, such as applying excessive force on a dense bone structure, can compromise the precision of the tool. Compliance with sterilization protocols ensures not only patient safety but also the longevity of the surgical instrumentation.

Who is the manufacturer and what standards are respected?

The #5 Black Line periotome is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a globally recognized manufacturer for the quality of its manual instrumentation. This product is classified as a Class I medical device. It is intended exclusively for professional use by dental surgeons, implantologists, or oral surgeons. Compliance with manufacturing standards ensures that the instrument meets safety and performance requirements for minor invasive procedures. Practitioners must systematically refer to the manufacturer's warnings to ensure use in accordance with current regulations.

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