Tunneling knife #2, short, Black Line

What is the #2 short Black Line tunneling knife?

The #2 tunneling knife, short version, belongs to the Black Line range developed by Hu-Friedy. This specialized instrument is designed for periodontal micro-surgery interventions. Its structure is distinguished by a specific dark coating that improves visual contrast with soft tissues and surrounding dental structures. As a precision instrument, it allows the surgeon to operate with increased visual clarity. This medical device is manufactured by Hu-Friedy Mfg. Co., LLC, a recognized manufacturer in the field of high-quality surgical instrumentation. Its design meets the requirements of practitioners performing meticulous gestures in periodontology and implantology.

What are the clinical indications for this dental micro-surgery instrument?

The intended use of this periodontal micro-knife primarily concerns tunneling techniques in periodontal plastic surgery. It is indicated for the creation of sub-mucosal tunnels during the treatment of gingival recessions by connective tissue graft. Its morphology allows for the detachment of the flap in partial thickness while preserving the integrity of the interdental papillae. This instrument is also relevant in root coverage procedures where atraumatic tissue management is crucial. In implant surgery, it can be used to prepare the site before the insertion of grafts or membranes, ensuring tissue manipulation adapted to micro-surgery protocols.

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

The #2 Black Line tunneling knife features technical characteristics optimized for access to restricted areas. Its short version offers increased maneuverability in posterior sectors or in patients with limited mouth opening. The Black Line finish is a distinctive feature of Hu-Friedy, providing a surface that reduces reflections under operating lights while increasing contrast with gingival tissues. Although the exact composition is not specified, manufacturing by Hu-Friedy Mfg. Co., LLC guarantees a high production standard for Class I instruments. The geometry of the blade is designed to allow precise incision and detachment without traumatizing adjacent structures.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy, contraindications are related to the intended use and general warnings for surgical instrumentation. This device is exclusively reserved for qualified healthcare professionals. Its use is contraindicated for any procedure other than those for which it was designed, notably outside of oral and periodontal surgery. Practitioners must refer to the instructions for use to identify specific clinical situations where the use of a sharp tunneling instrument might be inappropriate. Compliance with sterilization and maintenance protocols is imperative to avoid any risk of cross-complication or instrument failure during the surgical act.

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

As a reusable surgical instrument and not a suture, precautions relate to handling and the reprocessing cycle. The #2 tunneling knife must be inspected before each intervention to verify the integrity of its blade and its Black Line coating. It is imperative to read the instructions carefully before use to respect the cleaning and sterilization parameters recommended by Hu-Friedy. Careful handling is necessary to preserve the sharpness of the dental micro-surgery instrument. After each use, a rigorous decontamination protocol must be applied in accordance with current standards for Class I medical devices to ensure patient safety and the longevity of the tool.

Who is the manufacturer and what standards are respected?

The #2 tunneling knife, short, Black Line is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for its expertise in the design of high-precision dental instruments. As a Class I product, it meets the safety and performance requirements defined for this category of medical devices. Healthcare professionals must ensure the authenticity of the product and follow the manufacturer's guidelines to maintain the compliance of the instrument throughout its operational life in a dental office or hospital environment.

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