Distal Retentive Cutting Pliers 0.021 inch x 0.025 inch - Hu-Friedy - Delynov

What is the Hu-Friedy 0.021 x 0.025 distal cutter?

The Hu-Friedy distal cutter is a specialized instrument designed for the precise sectioning of orthodontic wires at the end of the arch. Manufactured by Hu-Friedy Mfg. Co., LLC, this plier is specifically sized to handle archwires up to a cross-section of 0.021 inch x 0.025 inch. Its structure is optimized for accessing the narrow posterior areas of the oral cavity. As a high-tech orthodontic instrumentation, it incorporates an essential safety mechanism for daily clinical practice, ensuring that the sectioned wire segment remains securely held by the instrument after cutting, thereby preventing any accidental ingestion or soft tissue injury to the patient.

What are the clinical indications for this plier?

The use of this ortho distal cutter is indicated during the adjustment and finishing phases of orthodontic treatments. It is primarily used to cut the excess wire protruding from tubes or bands at the molar level. Its design allows for a flush cut, minimizing patient discomfort related to cheek irritation from protruding archwire ends. It is suitable for rectangular and round archwires not exceeding 0.021 x 0.025 inch. This device is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-Friedy, for use in dental offices or specialized oral surgery hospital environments.

What are the technical characteristics of this instrument?

This Hu-Friedy plier is distinguished by its cutting capacity calibrated for wires with a maximum section of 0.021 inch x 0.025 inch. Its major technical feature lies in its retentive function, which grips the distal end of the wire simultaneously with the sectioning action. This double mechanical action ensures safe handling of orthodontic instrumentation in posterior sectors. The design of the cutting head is engineered to offer maximum visibility and facilitated access to difficult-to-reach areas. The manufacturing quality of Hu-Friedy Mfg. Co., LLC guarantees precise alignment of the jaws for a sharp and clean cut, reducing the manual effort required by the practitioner during device activation.

What are the contraindications for the use of this device?

According to the information provided by Hu-Friedy Mfg. Co., LLC, the use of this instrument is exclusively reserved for trained healthcare professionals. Contraindications include the use of the instrument on archwires whose dimensions or hardness exceed the technical specifications of 0.021 inch x 0.025 inch, which could irreparably damage the cutting edges of the plier. It is imperative not to use this device for functions other than cutting orthodontic archwires. Before each intervention, the practitioner must check the general condition of the instrument and the absence of residues, strictly following the indications and contraindications mentioned by the manufacturer located in Chicago, USA.

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

As a non-resorbable metallic instrument, the Hu-Friedy distal cutter requires a rigorous sterilization and maintenance protocol between each patient. Although specific material details are not specified, this type of orthodontic instrumentation must be cleaned, disinfected, and sterilized in accordance with the attached instructions for use. It is crucial to read the instructions carefully before use to preserve the mechanical cutting and retention properties. Storage must be in a dry environment to avoid any alteration. Compliance with the maintenance cycles recommended by Hu-Friedy ensures the longevity of the instrument and constant safety during surgical or orthodontic procedures.

Who is the manufacturer and what standards are met?

The plier is manufactured by Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a recognized manufacturer, Hu-Friedy subjects its products to strict quality controls to meet the needs of healthcare professionals. It is reminded that the use of this instrument is strictly reserved for practitioners and that a careful reading of the instructions is mandatory before any clinical implementation. This compliance with manufacturing standards ensures that the instrument meets the safety and performance requirements expected for Class I devices in orthodontics.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.