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Instrument for composite placement Gregg n°4/5 for molars class 2-4 - Hu-Friedy - Delynov

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The Instrument à composite Gregg #4/5 Molaires Classe 2-4 - 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.

50.85 € 50.85 EUR 50.85 € Tax Included

50.85 € Tax Included

(0.00 € / Units)
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Instrument

What is the Gregg #4/5 Molar Class 2-4 composite instrument?

The Gregg #4/5 composite instrument, manufactured by Hu-Friedy, is a specialized manual tool used in restorative dentistry. It belongs to the category of modeling instruments for aesthetic materials. Its double-ended structure allows the practitioner to manipulate composites with great dexterity. Designed by Hu-Friedy Mfg. Co., LLC, this instrument is specifically adapted to the requirements of posterior restorations, facilitating the placement and sculpting of filling materials in complex cavities. Its design is optimized to meet the needs of dental surgeons during the morphological reconstruction phase of molars.

What are the clinical indications for this Hu-Friedy instrument?

The Hu-Friedy Gregg #4/5 instrument is indicated for direct restoration procedures using composite resins. Its primary application concerns Class 2, Class 3, and Class 4 cavities on molars. In conservative surgery, it is used to condense composite material against cavity walls, remove excess, and sculpt occlusal or proximal anatomy. Its use is particularly relevant during the reconstruction of contact points and marginal ridges, where precise movement is decisive for the longevity of the restoration and the patient's periodontal health.

What are the technical characteristics of this instrument?

This Gregg #4/5 instrument is distinguished by its double-ended configuration, offering immediate versatility during the treatment session. Manufactured by Hu-Friedy Mfg. Co., LLC, it benefits from the manufacturing quality of a recognized manufacturer in the dental sector. Although exact material specifications are not detailed in the source data, this Class I instrument is designed for rigorous professional use. Its shape is specifically studied for access to posterior areas, allowing easy manipulation of the composite without excessive adhesion to the material, thus facilitating a homogeneous smoothing of restored surfaces.

What are the contraindications for the use of this instrument?

According to 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 standard safety protocols related to the use of manual instruments in the oral environment. Practitioners must systematically refer to the instructions for use before any intervention. As with any Class I device, compliance with sterilization and maintenance protocols is imperative to guarantee patient safety and the integrity of the instrument during clinical care.

What are the precautions for use and maintenance?

The Gregg #4/5 composite instrument is a non-resorbable device intended for repeated use after processing. Precautions for use include a visual inspection before each use to check for the absence of deformation or wear of the active tips. Being a Class I product, it must be cleaned, disinfected, and sterilized in accordance with the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC. Particular attention must be paid when cleaning hardened composite residues, as any accumulation can compromise modeling precision during subsequent uses. Compliance with recommended sterilization cycles ensures the longevity of the instrument.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by 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. As a Hu-Friedy product, it meets the manufacturing standards of a major player in dental instrumentation. Although specific CE marking is not mentioned in the source data, compliance with Class I indicates that it meets the essential safety and performance requirements for medical devices in this category. Healthcare professionals must imperatively read the manual before use to ensure compliance with the manufacturer's directives.


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Manufacturer Hu-Friedy
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