Lime Buck Number 11/12 with handle Number 523 - Hu-Friedy - Delynov

What is the Hu-Friedy Buck #11/12 file handle #523?

The Buck #11/12 file with #523 handle from the Hu-Friedy brand is a manual surgical instrument specifically designed for working on hard tissues in oral surgery. This device, manufactured by Hu-Friedy Mfg. Co., LLC, is a dental bone file used to refine and smooth bone surfaces. Its double-ended structure allows for precise manipulation during periodontology or implant surgery procedures. As a Class I device, it meets the regulatory requirements for non-invasive or invasive instruments for temporary use. The #523 handle offers a grip adapted to the requirements of practitioners for optimal control during the operative gesture.

What are the clinical indications for this dental bone file?

The Buck file is primarily indicated in periodontal surgery and bone surgery procedures. It is used by dental surgeons and implantologists for the resection and smoothing of irregular bone edges, notably after multiple dental extractions or during the preparation of an implant site. Its clinical application includes alveoloplasty, where it serves to regularize the alveolar ridge to facilitate soft tissue healing or the adjustment of a prosthesis. It is also effective for removing small bone spicules in difficult-to-access areas such as interproximal spaces, thus ensuring a flat bone surface that is non-traumatic for the flaps.

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

This Hu-Friedy instrument is distinguished by its Buck #11/12 configuration, mounted on a handle with reference #523. It is a double-ended active instrument, designed to maximize the efficiency of bone smoothing without changing tools. The design of the working parts allows for a controlled cutting or scraping action on the bone. Manufactured by Hu-Friedy Mfg. Co., LLC, this Class I medical device is intended to be sterilized and reused according to standard clinical protocols. Its manufacturing respects the rigorous quality standards of the manufacturer based in Chicago, ensuring the mechanical resistance necessary for the constraints of dental bone surgery.

What are the contraindications for the use of the Buck file?

According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific medical contraindications listed in the raw technical documentation, other than those related to the general use of surgical instruments in cases of serious systemic pathologies of the patient preventing oral surgical intervention. The practitioner must, however, ensure the absence of known allergies to the metallic components of the instrument, although the exact composition is not specified here. Inappropriate use on structures other than bone or dental hard tissues is prohibited to avoid damaging the active parts of the file.

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

As it is a metallic surgical instrument and not a suture, the notion of resorption does not apply. However, strict reprocessing precautions are necessary. The Hu-Friedy Buck #11/12 file must be cleaned, disinfected, and sterilized before each use in accordance with the manufacturer's instructions. It is imperative to read the instructions carefully before any handling. Like any bone cutting or smoothing instrument, the wear of the file's serrations must be checked regularly. A blunt instrument could compromise the precision of the surgical gesture and generate excessive heat on the bone tissue. Storage must be in a dry environment to preserve the integrity of the Class I device.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, headquartered 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 guarantees that the instrument is adapted to the requirements of professional dental surgery. Although specific CE marking is not mentioned in the source data, belonging to Class I indicates compliance with safety and performance rules for this category of devices. It is reminded that the use of this dental bone file is exclusively reserved for healthcare professionals trained in oral surgery techniques.

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