Ostéotome Bone-Shaver Number 1.32 Concave Right 3.2mm - Hu-Friedy - Delynov

What is the Bone-Shaver Osteotome #1.32 straight concave 3.2mm?

The Bone-Shaver Osteotome #1.32 is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device features a concave-shaped working end with a diameter of 3.2mm and a straight orientation. It is specifically designed for bone surgery interventions in implantology and periodontology. As a manual instrument, it allows the practitioner to exercise direct tactile control when modifying alveolar ridges or preparing recipient sites. This product belongs to the category of high-quality consumables and reusable instruments, meeting the requirements of specialized clinical environments.

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

The Bone-Shaver Osteotome #1.32 is indicated for various oral surgery procedures requiring precise bone manipulation. Its primary use includes implant site preparation, particularly for bone condensation in low-density bone to improve primary implant stability. The 3.2mm concave shape is particularly suited for crestal approach sinus floor elevation techniques (Summers technique), where the instrument serves to gently push the bone upward. It can also be used during ridge expansion or to regularize bone surfaces after an extraction. Its use is strictly reserved for qualified healthcare professionals.

What are the technical characteristics of this osteotome?

Technically, this Hu-Friedy instrument features a straight configuration, facilitating access to anterior and premolar areas. The specificity of this model lies in its 3.2mm diameter concave active part, designed to collect and compact bone chips during insertion. This geometry allows for optimal bone volume management without excessive material removal. Manufactured according to the rigorous standards of Hu-Friedy Mfg. Co., LLC, this instrument is designed to withstand repeated sterilization cycles in hospital or dental office environments. Its monoblock structure ensures direct transmission of the force applied by the surgeon, thus guaranteeing increased precision during osteotomy maneuvers.

What are the contraindications for the use of this instrument?

According to data from the manufacturer Hu-Friedy, the use of this osteotome is reserved exclusively for healthcare professionals trained in oral surgery techniques. Although specific contraindications are not detailed beyond the intended use, this instrument should not be used in situations where residual bone thickness is insufficient to support condensation forces, or in patients presenting general contraindications to implant surgery (uncontrolled coagulation disorders, severe metabolic bone pathologies). The practitioner must imperatively read the instructions for use carefully and evaluate the benefit-risk ratio for each patient before the intervention.

What are the maintenance and handling precautions?

As the Bone-Shaver Osteotome #1.32 is a Class I instrument, it requires a rigorous decontamination and sterilization protocol between each patient. Before the first use and after each intervention, the instrument must be cleaned, inspected for any signs of wear or deformation, and then sterilized according to the instructions from the manufacturer Hu-Friedy. Particular attention must be paid to the 3.2mm concave part to ensure the absence of organic residues. Handling must be performed with care to preserve the integrity of the active tip. In the event of a fall or visible damage, the instrument must no longer be used to guarantee patient safety and the success of the surgical procedure.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is 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. Hu-Friedy is a globally recognized manufacturer for the quality and reliability of its surgical instruments. Compliance with manufacturing standards ensures practitioners a tool that meets safety and performance requirements for oral surgery. As indicated on the labeling, the user must consult the instructions before any use. This product does not have a specified CE marking in the current source data, but it follows the strict manufacturing directives imposed on Class I medical devices.

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