Elevator Bayonet King Handle Number 510 - Hu-Friedy - Delynov

What is the Roy elevator handle #510 - Hu-Friedy - Delynov?

The Roy elevator handle #510 is a precision manual instrument manufactured by Hu-Friedy Mfg. Co., LLC. It consists of an active working part and an ergonomic handle referenced under number #510. This device is specifically designed for oral surgery interventions requiring delicate handling of hard tissues. As a Hu-Friedy brand instrument, it benefits from the expertise of a recognized manufacturer in the field of odontological instrumentation. This product belongs to the category of luxation instruments, used to mobilize dental structures before their final extraction, thus ensuring a methodical approach during surgical care.

What are the clinical indications?

This dental roy elevator is indicated for the luxation of teeth and the extraction of roots. In clinical practice, it is used by the surgeon to separate the tooth from its socket by exerting controlled pressure on the desmodontium. It proves particularly useful in cases of complex extractions, residual roots, or during the preparation of the alveolar site before implant placement. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons and stomatologists, intervening in contexts of oral surgery, periodontology, or implantology. The device allows for effective transmission of the force necessary to facilitate avulsion while respecting the integrity of the surrounding bone structures.

What are the technical characteristics?

The Roy elevator is distinguished by its handle #510, a specific configuration developed by Hu-Friedy to offer an optimal grip during force maneuvers. Although the exact details of the composition are not specified, the instrument is designed to meet the rigorous requirements of sterilization and durability in a surgical environment. It is a Class I device according to current regulations. The design of the working part is optimized to fit into the periodontal space, allowing the practitioner to apply an effective lever. Each unit is produced according to the quality standards of Hu-Friedy Mfg. Co., LLC, ensuring consistency in performance during each operative act.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not detailed beyond general warnings for use. However, the use of this straight root elevator must be avoided by anyone who does not have the qualification of a healthcare professional. It is imperative not to use the instrument for functions other than those intended by the manufacturer, such as levering on fragile prosthetic structures or non-bone tissues, which could damage the instrument or injure the patient. The practitioner must evaluate the clinical condition of the patient and bone density before any application of force to prevent the risk of unwanted alveolar fracture.

What are the precautions for use and maintenance?

As a non-resorbable and reusable instrument, this straight dental elevator requires a strict cleaning and sterilization protocol before each use. The manufacturer Hu-Friedy emphasizes the importance of carefully reading the instructions for use provided to ensure patient safety and device longevity. The integrity of the working part should be checked before each intervention to detect any signs of wear or deformation. Being a Class I device, it must be handled with care to maintain its mechanical properties. Storage must be in a dry and clean environment, in accordance with hospital and dental office standards, in order to avoid any cross-contamination or degradation of the material.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized for the high quality of its surgical instrumentation. The product is classified as a Class I medical device. Compliance with Hu-Friedy's rigorous manufacturing protocols ensures that the instrument meets the safety and performance requirements expected by healthcare professionals. Although specific CE marking is not mentioned in the source data, belonging to Class I indicates compliance with medical device classification rules for regulated marketing. Users must systematically refer to the official labeling for any additional information.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.