Davis Elevator Number 3 with Handle Number 503 - Hu-Friedy - Delynov

What is the Davis #3 elevator #502 handle - Hu-Friedy?

The Davis #3 elevator with #502 handle is a manual surgical instrument developed by the manufacturer Hu-Friedy Mfg. Co., LLC. This device is specifically designed for oral surgery procedures, particularly in the context of guided bone regeneration (GBR) and complex extractions. Its structure consists of a Davis #3 type working part mounted on an ergonomic handle referenced as #502, offering a grip adapted to the requirements of clinical practice. As a precision instrument, it allows for the application of necessary forces during luxation phases while respecting the integrity of surrounding tissues. This product embodies the expertise of Hu-Friedy, a recognized manufacturer in the field of high-quality dental instrumentation.

What are the clinical indications for this instrument?

The clinical indications for the Hu-Friedy Davis #3 elevator #502 handle primarily concern oral and implant surgery. It is indicated for the luxation of roots and teeth prior to extraction, as well as for the elevation of mucoperiosteal flaps during reconstructive procedures. In the context of guided bone regeneration (GBR), this instrument can be used to prepare the surgical site by delicately detaching soft tissues or mobilizing fine bone structures. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons, stomatologists, and implantologists, who have mastered the specific operative protocols for using elevators in the alveolar environment.

What are the technical characteristics of this elevator?

The Davis #3 elevator #502 handle is distinguished by its technical configuration optimized for fine surgery. The #502 handle is designed to ensure efficient transmission of manual force to the Davis #3 active tip. Although specific materials are not detailed in the provided technical documentation, Hu-Friedy manufacturing standards guarantee an instrument meeting Class I requirements. The geometry of the tip is designed to insert into the periodontal space, allowing for controlled leverage. This instrument is designed to withstand standard sterilization cycles in dental offices, in accordance with the instructions from the manufacturer Hu-Friedy Mfg. Co., LLC located in Chicago, USA.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively beyond general safety warnings. However, the use of this Davis #3 elevator is contraindicated for any use diverted from its primary function of oral surgery. It must not be used by unqualified persons, as its handling requires thorough knowledge of oral anatomy to avoid any bone fracture or nerve injury. It is also advisable to refer to the instructions for use to check for any contraindications related to the patient's systemic health status or potential allergies to the metal components of the instrument.

What are the precautions for use and maintenance?

As a non-resorbable Class I instrument, the Davis #3 elevator #502 handle requires strict precautions regarding sterilization and maintenance. Before each use, the practitioner must carefully read the instructions provided by Hu-Friedy. The instrument must be inspected for any signs of wear or deformation that could compromise patient safety. After the procedure, it must follow a protocol of cleaning, disinfection, and autoclave sterilization according to the recommended parameters for surgical instrumentation. Careful handling is required to preserve the sharpness of the Davis #3 tip and the integrity of the #502 handle, thus ensuring the longevity and performance of the tool during successive surgeries.

Who is the manufacturer and what standards are respected?

The Davis #3 elevator #502 handle is manufactured by Hu-Friedy Mfg. Co., LLC, with headquarters located at 3232 N. Rockwell St. Chicago, IL 60618, USA. This medical device is classified as Class I according to current regulations. The manufacturer Hu-Friedy is globally recognized for its compliance with rigorous quality standards in the production of surgical instruments. Although specific CE marking is not mentioned in the source data, the product complies with the regulatory requirements applicable to medical devices of its class. It is imperative for healthcare professionals to consult the instructions for use and respect the manufacturer's warnings to ensure practice consistent with current safety standards.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.