Bone chisel/Periosteal elevator #24G/13KL handle #6 short

What is the #24G/13KL Bone Chisel/Periosteal Elevator?

The #24G/13KL Bone Chisel/Periosteal Elevator marketed by the Hu-Friedy brand is a hybrid surgical instrument used in dentistry. It consists of a dual active part allowing for both cutting or reshaping bone and elevating soft tissue flaps. This specific model is mounted on a short #6 handle, optimizing the grip for practitioners during delicate interventions in the posterior zone or restricted spaces. As a Class I device, it meets the basic regulatory requirements for non-invasive or short-term invasive manual instrumentation, ensuring compliant integration into the surgical technical tray.

What are the clinical indications?

The clinical indications for this Hu-Friedy brand instrument primarily include oral surgery, implantology, and periodontology. It is used for periosteal elevation during the creation of full-thickness flaps, allowing for clear exposure of the surgical site. As a bone chisel, it is also used to smooth alveolar ridges after extraction or to prepare the bone bed before implant placement. Its dual function limits the number of instruments on the surgical field, thereby facilitating the flow of the surgical procedure during tissue and bone preparation phases.

What are the technical characteristics?

The #24G/13KL Bone Chisel/Periosteal Elevator is distinguished by its #24G/13KL technical configuration associated with a short-format #6 handle. The manufacturer Hu-friedy designed this instrument to offer a balance between robustness and maneuverability. The short handle is particularly suitable for hands of different sizes and allows for the application of controlled force during bone resection without compromising the tactile sensitivity necessary for soft tissue elevation. Although the exact composition is not specified, this Class I instrument is intended for strict professional use, respecting the manufacturing standards of a recognized manufacturer located in the USA.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-friedy, the use of this instrument is strictly reserved for qualified healthcare professionals. General contraindications include use by untrained personnel or for procedures not in accordance with the instrument's intended purpose (oral and bone surgery). It is imperative to consult the instructions before use to identify any specific contraindications related to the patient's pathology or particular clinical conditions that would make the use of manual instrumentation inappropriate. Compliance with sterilization and maintenance protocols is also a sine qua non condition to avoid any perioperative risk.

What are the precautions for use and maintenance?

As this Hu-Friedy brand instrument is a non-resorbable and reusable device, it requires rigorous precautions. Before each intervention, the practitioner must check the integrity of the active parts (chisel and elevator) to ensure the absence of corrosion or dullness. Manipulation must be precise to avoid damaging adjacent anatomical structures, such as neurovascular bundles. After use, cleaning, decontamination, and sterilization must be carried out in accordance with the instructions from the manufacturer Hu-friedy and the hygiene standards in force in the dental office. Particular attention must be paid to drying to preserve the mechanical properties of the short #6 handle.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. The manufacturer emphasizes that the use of this bone chisel/periosteal elevator is exclusively reserved for healthcare professionals. Compliance with manufacturing standards is ensured by the expertise of this globally recognized manufacturer in the dental sector. Although a specific CE marking is not mentioned in the source data, the Class I status indicates a level of regulatory control suitable for reusable manual surgical instruments, guaranteeing the safety and traceability of the product.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.