Periotome No. 3 Posterior Black Series Right Hu-Friedy Delynov

What is the Periotome #3, posterior, Black Line?

The Periotome #3 from the Black Line range by Hu-Friedy is a specialized surgical instrument designed for extraction procedures. It is distinguished by its specific configuration for the posterior zone and its right-sided orientation. This device belongs to the category of consumables (CONSO) and benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC. Its structure is optimized to fit into the periodontal space to break the ligament fibers before using elevators or forceps. The Black Line coating is a characteristic unique to this series of high-precision instruments, offering a response adapted to the requirements of dental surgeons and implantologists during oral surgery.

What are the clinical indications for the posterior periotome?

The posterior periotome is indicated in dental extraction protocols, particularly when an atraumatic approach is required to preserve the integrity of the alveolar bone, notably for immediate or delayed implantation. Its primary clinical use lies in the sectioning of the periodontal ligament at the level of the posterior teeth (molars and premolars). By facilitating the separation between the root and the bone, this instrument reduces the necessary luxation forces, thereby limiting the risk of fracture of the bone plates. It is exclusively reserved for healthcare professionals trained in oral and periodontal surgery techniques.

What are the technical characteristics of this instrument?

This specific model, the Periotome #3, features a geometry adapted to the anatomy of the right posterior sectors. Manufactured by Hu-Friedy Mfg. Co., LLC, it incorporates Black Line technology which improves the surface properties of the instrument. Its thin design allows for precise insertion into the sulcus and the ligament space without damaging the surrounding soft tissues. As a Class I device, it meets the standard regulatory requirements for non-invasive or reusable surgical instruments according to the specifications of the Chicago-based manufacturer. The shape of the handle and the working part is designed to offer optimal control during ligament sectioning maneuvers.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively beyond general usage warnings. However, the use of this posterior periotome is strictly reserved for qualified healthcare professionals. The instrument should not be used for excessive leverage functions that could lead to the bending or breaking of the thin working part. Practitioners must systematically refer to the instructions for use before any intervention to verify the suitability of the instrument with the patient's clinical state and the planned procedure.

What are the precautions for use and maintenance?

Although this product is not an absorbable suture, it requires rigorous precautions as a Class I surgical instrument. The manufacturer Hu-Friedy emphasizes the importance of carefully reading the instructions before use. Maintaining the integrity of the Black Line finish depends on compliance with the cleaning, disinfection, and sterilization protocols recommended by Hu-Friedy Mfg. Co., LLC. A visual examination of the instrument before each act is necessary to ensure the absence of deformation or premature wear. Handling must be precise and limited to ligament sectioning to ensure the longevity of the device and patient safety.

Who is the manufacturer and what standards are respected?

The Periotome #3 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. Hu-Friedy is a recognized manufacturer in the dental sector for the quality of its surgical instruments. The product is distributed by Delynov and must be used in accordance with the manufacturer's guidelines to ensure compliance with safety standards. Although specific CE marking is not detailed in the source data, the instrument meets the requirements for medical devices of its class for professional use in a clinical setting.

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Surgical medical consumables play a decisive role in operative safety.