Elevator Davis no. 10 with handle no. 503 - Hu-Friedy - Delynov

What is the Davis #10 elevator #2 handle?

The Davis #10 elevator #2 handle is a precision surgical instrument manufactured by Hu-Friedy Mfg. Co., LLC. This device belongs to the category of guided bone regeneration (GBR) instruments. It consists of an active part referenced as Davis #10 mounted on a #2 type handle, offering a grip adapted to the requirements of oral surgery. As a Hu-Friedy brand product, this elevator is designed to meet the needs of practitioners during delicate tissue or bone manipulations. Its structure is optimized to ensure efficient force transmission during clinical procedures in private practice or hospital environments.

What are the clinical indications?

The intended use of this instrument is strictly reserved for healthcare professionals trained in oral surgery techniques. The Davis #10 elevator is primarily indicated in oral surgery protocols, notably for flap elevation or the manipulation of structures during guided bone regeneration phases. It is used in clinical contexts where precise tissue mobilization is necessary to expose the surgical site or prepare for the insertion of filling materials. The manufacturer Hu-Friedy specifies that use must comply with the indications and contraindications mentioned in the official technical documentation accompanying the device.

What are the technical characteristics?

This instrument is distinguished by the combination of a Davis #10 tip and an ergonomic #2 size handle. Manufactured by Hu-Friedy Mfg. Co., LLC, this elevator is classified as a Class I medical device according to current regulations. Although specific details on the exact material composition are not provided in the source data, Hu-Friedy manufacturing standards ensure quality suitable for reusable surgical instrumentation. The #2 handle is designed to offer optimal control during leverage or detachment movements, minimizing fatigue during prolonged implant or periodontal surgery interventions.

What are the contraindications for use?

Specific contraindications related to the use of the Davis #10 elevator are defined by the manufacturer Hu-Friedy. In accordance with safety warnings, this device is exclusively reserved for qualified healthcare professionals. Its use is contraindicated outside the intended surgical framework or by persons not trained in oral instrumentation techniques. It is imperative to refer to the instructions for use and guidelines provided by Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA before any intervention. Any clinical situation that does not allow for a safe application of the instrument constitutes a contraindication to its immediate use.

What are the precautions for use and maintenance?

As a non-resorbable instrument intended for surgery, the Davis #10 elevator requires rigorous preparation before each procedure. Professionals must carefully read the manual before use to ensure patient safety and instrument longevity. As with any Class I Hu-Friedy device, a cleaning, disinfection, and sterilization protocol must be applied according to the manufacturer's directives. The integrity of the Davis #10 tip and the #2 handle should be checked before each intervention. Compliance with recommended sterilization cycles is essential to maintain the functional properties of the steel and prevent risks of cross-contamination.

Who is the manufacturer and what standards are respected?

The Davis #10 elevator #2 handle is manufactured by Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is listed as Class I, which corresponds to basic surgical instruments presenting a low potential risk to the patient while requiring strict compliance with safety and performance requirements. Hu-Friedy is a globally recognized manufacturer in the dental sector for the quality of its instrumentation. Compliance with Medical Device Regulations (MDR) ensures that the instrument meets the manufacturing standards required for professional use in a surgical environment.

State of the art

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