V-Stop V-shaped Stopper Clamp 0.022 inch x 0.025 inch - Hu-Friedy - Delynov

What are the Hu-Friedy V-stop pliers?

The Hu-Friedy V-stop pliers are a precision instrument designed specifically for practitioners involved in orthodontics and oral surgery. Manufactured by Hu-Friedy Mfg. Co., LLC, these pliers allow for specific folds on archwires with maximum dimensions of 0.022 inch x 0.025 inch. Their structure is optimized to guarantee reliable handling when shaping retention devices. As a Class I instrument, they meet the basic regulatory requirements for non-invasive medical devices. This device is an essential tool for clinicians seeking to secure archwire positioning without compromising material integrity.

What are the clinical indications for this instrument?

These V-stop pliers are primarily indicated for the creation of stop folds (V-stops) on orthodontic archwires. In oral surgery and implantology, they are used to adjust stabilizing archwires or guidance devices during pre-surgical orthodontic preparation phases. The clinical objective is to prevent the archwire from sliding through brackets or tubes, thereby ensuring constant force and stable positioning of teeth or bone segments. Their use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-Friedy based in Chicago.

What are the technical characteristics of the V-stop pliers?

The orthodontic V-stop pliers feature technical characteristics calibrated for archwire sections up to 0.022 inch x 0.025 inch. The geometry of the jaws is designed to imprint a clean and precise V-shaped fold without weakening the metallic structure of the archwire. The mechanical design ensures optimal force transmission, allowing the practitioner to create the fold with minimal effort. This Hu-Friedy instrument is classified in the GBR (Guided Bone Regeneration) category at Delynov, highlighting its utility in complex protocols where dental and bone stability is paramount for the success of grafts and implant placement.

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 reserved exclusively for healthcare professionals. There are no specific medical contraindications listed other than inappropriate use by unqualified personnel. However, it is imperative not to use these pliers on archwires whose dimensions exceed 0.022 inch x 0.025 inch, as this risks damaging the instrument's jaws or causing archwire breakage. The practitioner must carefully read the instructions for use and respect standard sterilization protocols before any intraoral intervention.

What are the maintenance and handling precautions?

Although this product is not an absorbable suture, its durability depends on compliance with cleaning and sterilization cycles. Like any Class I instrument from the Hu-Friedy brand, it must be inspected before each use to check for the absence of corrosion or jaw deformation. The archwire bending pliers must be handled with care to preserve the precision of the folding mechanism. Regular lubrication of the joints is recommended to maintain smooth movement. Compliance with the manufacturer's warnings located at 3232 N. Rockwell St. Chicago is essential to ensure patient safety and the longevity of the surgical instrumentation.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, IL 60618 USA. This product is classified as a Class I medical device. Hu-Friedy is a globally recognized manufacturer for the quality of its manual instrumentation. Compliance with American and international manufacturing standards ensures practitioners a reliable tool for their daily interventions. It is reminded that the use of these ortho bending pliers must take place within a strict clinical framework, following the indications and contraindications provided by the manufacturer in the accompanying instructions.

State of the art

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