Sugarman File #3S/4S handle #2 - Hu-Friedy - Delynov

What is the Sugarman #3S/4S file handle #2 - Hu-Friedy?

The Sugarman #3S/4S file mounted on a #2 handle is a high-precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device, belonging to the category of periodontal surgery instruments (INSTRU), is specifically designed for work on hard tissues. As a periodontal bone file, it features a structure adapted to the requirements of modern periodontology. This Sugarman model is recognized for its double configuration, allowing efficient handling during the treatment of bone surfaces. Its design meets the quality standards of a recognized manufacturer like Hu-Friedy, ensuring optimal integration into the instrument sets of clinics specialized in oral and periodontal surgery.

What are the clinical indications for this periodontal file?

The dental Sugarman file is primarily indicated for periodontal surgery interventions requiring bone remodeling or smoothing. It is used by healthcare professionals for the removal of bone spicules, the regularization of alveolar ridges after extraction, or during flap surgeries. Its use is also relevant for the removal of extremely dense subgingival calculus deposits that standard curettes cannot break. In implant surgery, it can be used to prepare the recipient site by refining the bone topography. This device is strictly reserved for qualified healthcare professionals mastering oral surgery techniques.

What are the technical characteristics of this instrument?

The Sugarman #3S/4S file is characterized by its #2 type handle, offering a grip adapted to repetitive scraping and smoothing movements. Although the exact composition is not specified in the provided technical data, this instrument benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. It is a Class I medical device, which implies compliance with basic regulatory requirements for non-invasive or reusable surgical instruments after sterilization. The reference #3S/4S defines the specific morphology of the working ends of the file, optimized to access different faces of the roots and alveolar bone structures.

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

According to information from the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for healthcare professionals. General clinical contraindications apply, notably the use on tissues that do not present the required indications for bone remodeling or periodontal smoothing. It is imperative not to use the instrument if it shows marked signs of wear or structural damage that could compromise patient safety or the effectiveness of the surgical act. The practitioner must systematically refer to the instructions for use and current clinical protocols to ensure the match between the patient's health status and the planned intervention.

What are the maintenance and handling precautions?

Like any Class I instrument intended for surgery, the Sugarman #3S/4S file must be subject to a rigorous cleaning, disinfection, and sterilization protocol before each use. Although resorption details do not apply here (as it is an instrument and not a suture), the durability of the file depends on compliance with the sterilization cycles recommended by Hu-Friedy. It is advised to read the instructions carefully before use to become aware of the manufacturer's specific warnings. A visual inspection of the working surfaces is recommended to guarantee that the cutting and smoothing capabilities of the periodontal file remain optimal for surgical procedures.

Who is the manufacturer and what standards are respected?

The Sugarman #3S/4S file is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for the quality of its surgical instruments and respects the strict manufacturing standards imposed by American and international health authorities. Although the specific CE marking is not mentioned in the technical sheet, compliance with Class I requirements ensures that the instrument meets the safety and performance standards for professional use in dental practices and hospital environments.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.