Periodontal Int Esthetic Tip #10 Mesial/Distal Angled - Hu-Friedy Delynov

What is the Hu-Friedy Int. Periotome Tip #10 Mesial/Distal Angulated?

The Int. Periotome Tip #10 Mesial/Distal Angulated, designed by Hu-Friedy, is a specialized extraction instrument used in oral surgery. This device is distinguished by its specific configuration allowing intervention in the mesial and distal areas of the tooth. Unlike traditional elevation instruments, this tip is structured to insert into the narrow ligament space. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument meets the requirements of practitioners seeking tools adapted to atraumatic extraction protocols. It is an essential component for surgeons wishing to limit damage to surrounding soft and hard tissues before implant placement or bone grafting.

What are the clinical indications for the distal and mesial periotome?

The clinical indications for this distal and mesial periotome primarily concern tooth extractions where preservation of the bone plate is critical. It is used to sever the fibers of the periodontal ligament (desmodontium) on the proximal faces of the roots. Its use is particularly recommended during pre-implant surgeries to maintain intact alveolar architecture. By facilitating the separation of the root from its bony attachment, this instrument allows for gentler luxation, thereby reducing the need for excessive force when using forceps. It is exclusively reserved for healthcare professionals trained in oral and periodontal surgery techniques.

What are the technical characteristics of this Hu-Friedy instrument?

This Class I medical device features technical characteristics specific to the Hu-Friedy range. The #10 tip has an optimized angulation for mesial and distal sectors, offering ergonomics adapted to difficult clinical access. Its design allows precise insertion into the sulcus to reach the ligament without compressing the alveolar walls. The technical reference indicates use as an interchangeable or integrated tip, depending on the handle system used. As a Class I product, it complies with basic regulatory requirements for non-invasive or short-term invasive surgical instruments. The manufacturing quality of Hu-Friedy Mfg. Co., LLC ensures a fine tactile response when handling periodontal tissues.

What are the contraindications for the use of this angulated periotome?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond the general scope of intended use. However, the use of this angulated periotome is strictly reserved for qualified healthcare professionals. It must not be used for heavy leverage functions, as its technical thinness is intended for ligament sectioning and not massive bone elevation, which could damage the instrument or anatomical structures. The practitioner must systematically refer to the instructions for use before any intervention to check the suitability of the tool with the patient's clinical status and the planned procedure.

What are the maintenance and handling precautions?

As a reusable Class I surgical instrument, rigorous precautions must be observed. Although resorption details do not apply here as it is not an implantable material, maintaining the integrity of the tip is crucial. Cleaning, disinfection, and sterilization must follow Hu-Friedy standard protocols to ensure patient safety and instrument longevity. It is imperative to read the instructions carefully before use. Handling must be precise to avoid any fracture of the fine end during insertion into the periodontal space. A visual check of the tip before each act is necessary to detect any deformation or premature wear.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified as a Class I medical device. Compliance with manufacturing standards by Hu-Friedy ensures that the instrument meets safety and performance requirements for professional use in a surgical environment. Specific CE marking is not mentioned in the source data, but compliance with current regulations for Class I devices is implicit for its marketing. Practitioners must ensure the authenticity of the product by sourcing from authorized distributors like Delynov to guarantee the traceability and quality of the equipment used.

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