Osteotome Bone-Pusher #5.50 bayonet 5.0mm cylin. - Hu-Friedy - Delynov

What is the Hu-Friedy #5.50 Bone-Pusher Osteotome?

The #5.50 Bone-Pusher Osteotome, manufactured by Hu-Friedy Mfg. Co., LLC, is a specialized surgical instrument used for the manipulation of bone grafts. This device is distinguished by its bayonet structure and its 5.0mm cylindrical tip. Designed to meet the requirements of dental surgeons and implantologists, this instrument allows for precise control during the positioning of filling materials. As a product in the CONSO category at Delynov, it benefits from the manufacturing expertise of Hu-Friedy, a recognized leader in the dental instrumentation sector. This device is classified as a Class I instrument according to current regulations, guaranteeing its compliance for professional use in dental offices or hospital settings.

What are the clinical indications for this bone pusher?

The Hu-Friedy bayonet bone pusher is primarily indicated for pre-implant surgery and periodontology interventions requiring the addition of filling material. Its use is recommended for the compaction of autogenous, allogeneic, or synthetic bone, particularly during maxillary sinus elevation procedures (sinus lift) or extraction socket filling. The specific design of this instrument allows the practitioner to exert controlled axial pressure, ensuring optimal material density within the bone defect. Its use is strictly reserved for healthcare professionals trained in oral surgery techniques, in accordance with the directives provided by the manufacturer Hu-Friedy Mfg. Co., LLC located in Chicago, USA.

What are the technical characteristics of the instrument?

The instrument features precise technical specifications to meet the constraints of oral anatomy. It has a cylindrical tip with a diameter of 5.0mm, a size adapted to intermediate-sized cavities. Its bayonet shape is a major feature that allows the handle axis to be offset from the working axis, thus offering increased visibility and easier access to the posterior areas of the oral cavity without interfering with adjacent dental structures. This bone pusher is a Class I device, manufactured by Hu-Friedy, guaranteeing the robustness necessary for repeated bone condensation maneuvers. Every technical detail is designed to ensure effective force transmission during clinical application.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no specific medical contraindications listed other than those related to general oral surgery protocols. However, the use of this instrument is prohibited for any application other than that intended by the manufacturer, namely bone compaction. The practitioner must ensure the absence of local or systemic pathologies in the patient that would contraindicate bone augmentation surgical intervention. It is imperative to read the instructions for use carefully before any manipulation to ensure patient safety and instrument integrity.

What are the precautions for use and maintenance?

As a Class I instrument, the Hu-Friedy #5.50 Bone-Pusher Osteotome requires a strict protocol of cleaning, disinfection, and sterilization between each patient. Before use, the professional must inspect the instrument to check for the absence of visible damage on the 5.0mm cylindrical tip or on the bayonet body. Particular attention must be paid during compaction to avoid excessive pressure that could damage the surrounding bone walls or the graft material. Compliance with the sterilization cycles recommended by Hu-Friedy is essential to maintain the mechanical properties of the steel and prevent risks of cross-contamination. The accompanying instructions detail all the warnings necessary for safe practice.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St., Chicago, IL 60618, USA. It is a Class I medical device, which implies compliance with basic regulatory requirements for non-invasive or reusable surgical instruments. Hu-Friedy is a globally recognized manufacturer for the quality of its dental instruments. The product is distributed by Delynov and must be used in accordance with the indications and warnings provided by the manufacturer. Although specific CE marking is not mentioned in the source data, the Class I classification confirms its status as a regulated medical device intended exclusively for professional use by competent healthcare practitioners.

State of the art

Surgical medical consumables play a decisive role in operative safety.