Apical Elevator Howard No.4 with Handle No. 502 - Hu-Friedy - Delynov

What is the Howard #4 apical elevator with #502 handle?

The Howard #4 apical elevator with #502 handle is a manual instrument designed by the manufacturer Hu-Friedy, recognized for its expertise in surgical instrumentation. This device consists of a specific active part, the Howard #4 model, mounted on an ergonomic #502 type handle. It is primarily used in oral surgery to facilitate the extraction of roots and root debris. As a precision instrument, it meets the requirements of practitioners for the luxation of dental structures. This product is classified as a Class I medical device, guaranteeing its compliance with basic regulatory standards for non-invasive or reusable instruments after sterilization.

What are the clinical indications?

The clinical indications for this Hu-Friedy apical elevator essentially concern exodontia procedures. It is indicated for the mobilization, luxation, and extraction of dental roots or root fragments remaining in the socket. Its Howard #4 design is particularly suitable for reaching apical areas and exerting controlled force to break ligament fibers. This instrument is used during conventional or complex dental surgeries, including extractions prior to implant placement. Its use is strictly reserved for qualified healthcare professionals, such as dentists, stomatologists, and implantologists, in accordance with the directives of the manufacturer Hu-Friedy Mfg. Co., LLC.

What are the technical characteristics of this instrument?

The Howard #4 elevator is distinguished by its specific technical configuration combining a refined working tip and a #502 type handle. The #502 handle is designed to provide a stable grip and allow for optimal transmission of force during the lever maneuvers necessary for apical elevation. Manufactured by Hu-Friedy, this instrument benefits from the manufacturing standards of the Chicago-based company. Although the exact composition is not specified in the provided technical documentation, instruments in this category are generally designed to withstand repeated sterilization cycles in a clinical environment. This device is a Class I instrument, which implies rigorous monitoring of cleaning and maintenance protocols by the dental office.

What are the contraindications for use?

According to the information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond general warnings of intended use. However, the use of this apical elevator is contraindicated for any person who does not have the qualification of a healthcare professional. It must not be used outside the surgical framework for which it was designed. Practitioners must assess the usual clinical risks associated with dental extraction, such as proximity to sensitive anatomical structures (alveolar nerve, maxillary sinus). It is imperative to read the instructions carefully before use to ensure that the patient's clinical condition does not present a contraindication to an invasive surgical intervention.

What are the maintenance and safety precautions?

As a Class I instrument intended for professional use, the Hu-Friedy Howard #4 elevator requires a strict maintenance protocol. Before the first use and after each intervention, the instrument must be cleaned, disinfected, and sterilized in accordance with the instructions in the manual and the hygiene standards in force in dental surgery. It is essential to check the integrity of the Howard #4 tip and the #502 handle before each act to avoid any risk of breakage or injury. The manufacturer's warnings remind that this device is reserved for healthcare professionals. Inadequate handling or excessive force could damage the alveolar bone or the instrument itself, compromising patient safety.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, whose headquarters is located at 3232 N. Rockwell St. Chicago, Il 60618 USA. Hu-Friedy is a historical and recognized player in the field of global dental instrumentation. This product is listed under Class I according to medical device regulations. Although specific CE marking is not mentioned in the source data, compliance with US and international regulatory requirements for Class I devices is ensured by the manufacturer's quality processes. Healthcare professionals must refer to the indications and contraindications provided by Hu-Friedy and read the instructions carefully to guarantee use in accordance with current safety standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.