Osteotomy Bone Spreader Number 2.37 Convex Straight 3.7mm - Hu-Friedy

What is the Bone-Spreader Osteotome #2.37 straight convex 3.7mm?

The Bone-Spreader Osteotome #2.37 is a high-precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device is characterized by a convex and straight working end, featuring a diameter of 3.7mm. Designed for bone surgery interventions, this instrument from the CONSO category is intended to manipulate alveolar structures. Its rigid structure allows for efficient force transmission during expansion maneuvers. As a Hu-Friedy product, it benefits from the expertise of a recognized manufacturer in the field of medical instrumentation, guaranteeing a response adapted to the requirements of specialized operating blocks in implantology and oral surgery.

What are the clinical indications for this instrument?

This instrument is primarily indicated for ridge expansion and bone condensation procedures in implant surgery. The use of the Hu-Friedy convex Bone-Spreader Osteotome #2.37 is relevant when the horizontal bone volume is insufficient to receive an implant in a standard manner. By percussing or inserting the instrument, the practitioner can spread the cortical walls and condense the cancellous bone, thereby improving the quality of the recipient site. It is specifically designed for clinical cases requiring a 3.7mm preparation diameter, allowing for an atraumatic approach compared to traditional drilling techniques that remove precious bone substance.

What are the technical characteristics of this osteotome?

The Bone-Spreader Osteotome #2.37 presents rigorous technical specifications to meet the needs of surgeons. Its convex tip is calibrated at 3.7mm, offering an optimized contact surface for the distribution of mechanical stress on the bone walls. The straight configuration of the instrument ensures precise axial alignment during insertion in anterior or accessible sectors. Manufactured by Hu-Friedy, this device belongs to Class I of medical devices. The design of the instrument aims to offer a fine tactile response to the practitioner, essential for assessing bone resistance and preventing the risks of fracture during alveolar expansion.

What are the contraindications for the use of this device?

The use of the Hu-Friedy Bone-Spreader Osteotome #2.37 is strictly reserved for qualified healthcare professionals. Contraindications include all clinical situations where the bone presents excessive fragility or insufficient density that does not allow for safe expansion. Although the detailed specifications do not list specific biological contraindications in the provided documentation, the practitioner must refer to standard surgical protocols regarding systemic pathologies that may affect bone healing. It is imperative to read the instructions carefully before use to ensure the adequacy between the patient's physiological state and the planned osteotomy technique.

What are the precautions for use and maintenance?

As a Class I device, this Hu-Friedy instrument requires rigorous handling. The manufacturer, Hu-Friedy Mfg. Co., LLC, emphasizes that use is exclusively reserved for healthcare professionals. Before each intervention, it is crucial to check the integrity of the 3.7mm tip and the absence of deformation of the instrument body. Sterilization and cleaning must be carried out in accordance with current protocols for reusable surgical instrumentation, although the specific treatment method must be validated by the manufacturer's instructions. Particular attention must be paid to preserving the convex profile to maintain clinical efficacy during bone expansion.

Who is the manufacturer and what standards are respected?

The Bone-Spreader Osteotome #2.37 is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a manufacturer recognized for the quality of its surgical instruments worldwide. This product complies with the regulations for Class I medical devices. Compliance with this classification ensures that the device meets the essential safety and performance requirements defined for this category. Healthcare professionals must refer to the indications and warnings provided by the manufacturer to ensure use in compliance with current safety standards during surgical procedures.

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