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Old Style Loop Pliers 0.022 inch x 0.025 inch - Hu-Friedy - Delynov

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The Pince Old Style Loop<=0.022 inch x 0.025 inch - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.

  • Compliance: Medical device Class I.
  • Manufacturer: Hu-Friedy Mfg. Co., LLC.
  • Reserved for healthcare professionals. Read instructions carefully before use.

204.00 € 204.0 EUR 204.00 € Tax Included

204.00 € Tax Included

(0.00 € / Units)
  • Manufacturer

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Instrument

What are the Hu-Friedy Old Style Loop pliers?

The Old Style Loop pliers from the brand Hu-Friedy are a specialized manual instrument used primarily for the manipulation of archwires. This device is designed to work with wires whose dimensions can reach up to 0.022 inch x 0.025 inch. Manufactured by Hu-Friedy Mfg. Co., LLC, these orthodontic loop pliers meet the requirements of practitioners seeking a reliable tool for standardized loop forming. Its structure is adapted to the mechanical stresses associated with bending common orthodontic alloys, ensuring optimal force transmission during the shaping of loops on the archwire.

What are the clinical indications for this instrument?

These ortho loop forming pliers are indicated for the creation of closing loops, leveling loops, or any other intraoral or extraoral adjustment requiring clean wire bending. They are particularly used in fixed orthodontics to customize finishing archwires. Their use is reserved for qualified healthcare professionals, such as orthodontists and dental surgeons, involved in the treatment of malocclusions or complex dental realignments. They allow for the precise management of orthodontic wire loops necessary for the activation of mechanical forces on dental units.

What are the technical characteristics of the Old Style Loop pliers?

The Old Style Loop pliers feature specific dimensional characteristics to accept rectangular or square wires up to 0.022 inch x 0.025 inch. The geometry of its jaws is designed to allow regular bending without nicking or weakening the metal of the archwire. As a Hu-Friedy product, this instrument benefits from the expertise of the manufacturer based in Chicago. The ergonomic design of the handles allows for a stable grip, essential for achieving symmetrical and precise bends. This device belongs to the GBR (Guided Bone Regeneration) category within the Delynov catalog, although its primary function is technical orthodontics.

What are the contraindications for the use of these pliers?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for trained healthcare professionals. There are no specific clinical contraindications listed other than those related to inappropriate use of the tool, such as bending wires whose section exceeds the technical capacity of 0.022 x 0.025 inch, which could damage the jaws. Practitioners must refer to the indications and contraindications mentioned in the accompanying instructions before any intervention on the patient to ensure treatment safety.

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

As a reusable and non-resorbable surgical instrument, the orthodontic loop pliers must undergo a rigorous cleaning, disinfection, and sterilization protocol between each patient. Although specific material details are not provided, Hu-Friedy instruments generally require maintenance in accordance with dental standards to prevent corrosion and maintain the integrity of the joints. It is imperative to read the manufacturer's instructions carefully before use to know the recommended sterilization cycles and ensure the longevity of the pliers when bending orthodontic wires.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This medical device is classified as Class I according to current regulations. Hu-Friedy's compliance with manufacturing standards ensures that the instrument meets safety and performance requirements for professional use in a dental office or hospital setting. Although CE marking is not specified in the source data, the Class I classification confirms its status as a regulated medical device, requiring traceability and compliance with the use procedures defined by the manufacturer.


State of the art

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

Specifications

Manufacturer Hu-Friedy
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