Steiglitz Fragment Forceps 90° 12 cm - Hu-Friedy - Delynov

What is the Hu-Friedy Steiglitz 90° 12 cm fragment forceps?

The Steiglitz 90° 12 cm fragment forceps, designed by the manufacturer Hu-Friedy, is a specialized surgical instrument used in oral and implant surgery. This device is distinguished by its working part angled at 90 degrees, offering a specific angulation to intervene in clinical areas where direct access is limited. With a total length of 12cm, it allows for fine and precise manipulation. Manufactured by Hu-Friedy Mfg. Co., LLC, this forceps is a robust tool intended for gripping small elements. It belongs to the category of guided bone regeneration (GBR) and alveolar surgery instruments, meeting the requirements of practitioners for managing debris during operative acts.

What are the clinical indications for this instrument?

This steiglitz forceps is primarily indicated for grasping and extracting fragments during oral surgery procedures. It is particularly useful for removing a root fragment forceps or fractured apices remaining in the socket after tooth extraction. Its use extends to the recovery of small bone fragments, filling material debris, or foreign bodies present in the surgical site. In minimally invasive endodontic surgery or implantology, it allows for cleaning the surgical site before placing an implant or regeneration material. Its 90° design is a major asset for reaching the posterior areas of the oral cavity or narrow alveolar floors.

What are the technical characteristics of the Hu-Friedy forceps?

The Steiglitz fragment forceps from Hu-Friedy presents precise technical specifications to meet the needs of surgeons. It measures 12cm long, a compact dimension that promotes tactile control during delicate movements. Its main characteristic lies in its active end oriented at 90°, which allows bypassing anatomical obstacles and accessing deep roots or fragments. As a Hu-Friedy product, it benefits from the manufacturing expertise of Hu-Friedy Mfg. Co., LLC, guaranteeing a finish quality adapted to hospital and office sterilization protocols. This instrument is classified as a Class I medical device, which frames its professional use and basic regulatory compliance.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is strictly reserved for qualified healthcare professionals. There are no specific listed medical contraindications other than those related to standard surgical protocols in oral surgery. However, the use of the root fragment forceps should be avoided if the practitioner does not have the necessary visibility or if the space is insufficient for the insertion of the instrument without risking damage to the surrounding soft tissues or adjacent nerve structures. It is imperative to read the instructions carefully before use to respect the safety warnings and the general indications and contraindications of the manufacturer located in Chicago, USA.

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

The Steiglitz fragment forceps is a non-resorbable and reusable metallic instrument. To maintain its gripping performance, particularly for a root fragment forceps, it must undergo a complete cycle of decontamination, cleaning, and sterilization after each use, in accordance with Hu-Friedy guidelines. It is advised to regularly inspect the alignment of the 90° jaws and the condition of the hinge to ensure the absence of corrosion or material fatigue. Rigorous maintenance guarantees the longevity of the instrument and patient safety during repeated interventions. As this device is Class I, it must be handled with care to avoid any deformation of the tips that would compromise the precision of fragment grasping.

Who is the manufacturer and what standards are met?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed under Class I, which corresponds to reusable surgical instruments according to current regulations. Although specific CE marking is not mentioned in the source data, the product complies with the rigorous manufacturing standards of Hu-Friedy, a recognized player in the global dental sector. Healthcare professionals should refer to the instructions provided by the manufacturer to ensure compliant use. The labeling specifies that the product is exclusively reserved for healthcare professionals, highlighting the importance of adequate training for its handling in surgery.

State of the art

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