Hu-Friedy dental extraction forceps #217 lower 1st-2nd molars - Hu-Friedy - Delynov

What is the Hu-Friedy #217 lower 1-2 molar forceps?

The Hu-Friedy #217 forceps is a manual surgical instrument intended for dental extraction. Manufactured by Hu-Friedy Mfg. Co., LLC, this device is specifically configured to adapt to the anatomy of the lower molars, specifically the first and second molars. Its structure is designed to meet the requirements of practitioners during avulsion procedures in the mandible. As an instrument in the CONSO category at Delynov, it fits into the standard oral surgery protocol for the removal of dental organs whose preservation is no longer possible or indicated.

What are the clinical indications?

The clinical indications for the Hu-Friedy #217 forceps primarily concern the extraction of the first and second lower molars. This instrument is used by dental surgeons and implantologists during simple or complex exodontia procedures. It is used when the tooth presents major carious degradation, terminal periodontal pathology, or as part of an implant treatment plan requiring conditioning of the alveolar site. Its use is strictly reserved for qualified healthcare professionals mastering mandibular extraction techniques to ensure optimal patient care.

What are the technical characteristics?

The Hu-Friedy #217 forceps is characterized by an architecture adapted to the morphology of the lower 1 and 2 molars. The design of its beaks allows for precise adaptation to the neck of the tooth, ensuring effective transmission of forces during the rotation or tilting movements necessary to rupture the alveolar-dental ligament. This device is a reusable instrument, regulatory classified as Class I according to current directives. Like all products from the Hu-Friedy brand, it benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, based in Chicago, guaranteeing a tool that complies with the needs of general practice and specialized surgery.

What are the contraindications for use?

The contraindications for the use of the Hu-Friedy #217 forceps are not specifically listed exhaustively in the provided technical documentation, beyond the general warnings related to oral surgery. Generally, the use of this instrument is contraindicated in patients presenting uncontrolled systemic pathologies that could interfere with healing or hemostasis, or in the absence of a clinical indication for extraction. It is the practitioner's responsibility to evaluate the benefit/risk ratio before any intervention and to consult the instructions for use provided by the manufacturer to be aware of specific warnings.

What are the maintenance and durability precautions?

Although resorption details do not apply to this non-resorbable instrument, the durability of the Hu-Friedy #217 forceps depends on its rigorous maintenance. As a Class I device, it must be cleaned, disinfected, and sterilized before each use in accordance with current protocols in dental offices or hospital settings. Professionals must read the instructions carefully before use to respect the sterilization cycles recommended by Hu-Friedy. Regular visual inspection of the beaks and the joint is necessary to ensure the absence of corrosion or deformation that could compromise the safety of the surgical act.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is the company Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St., Chicago, IL 60618, USA. The Hu-Friedy #217 forceps is a Class I medical device. Compliance with manufacturing standards by Hu-Friedy ensures practitioners a reliable instrument for their daily interventions. It is reminded that this product is exclusively reserved for healthcare professionals. Compliance with indications and maintenance protocols is essential to guarantee the conformity of the device throughout its operational life within the dental surgery technical platform.

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