Flohr dental root elevator, curved, figure 2 - Helmut Zepf (17.010.02) - Delynov

What is the Flohr dental root elevator, curved, figure 2?

The Flohr dental root elevator, bearing reference 17.010.02, is a manual instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device consists of a handle and a curved active shank, specifically designed for extraction procedures. Its structure allows for the application of precise mechanical force during root luxation. As an instrument in the Helmut Zepf range, it meets the quality requirements of German manufacturing for surgical instrumentation. This flohr elevator is a standardized tool used by dental surgeons to facilitate the avulsion of teeth or root debris that are difficult to access.

What are the clinical indications for this Helmut Zepf instrument?

This flohr dental elevator is primarily indicated in oral surgery for the extraction of roots or single teeth. Its curved configuration, corresponding to figure 2, is particularly useful for accessing areas where a straight instrument would not allow for an optimal angle of attack. It is used to separate the tooth from its alveolar attachment by inserting the tip into the periodontal space. The clinical objective is to mobilize the root before using forceps or to finalize the extraction of roots fractured below the crestal level. Its use is part of simple or complex extraction protocols, including preparations for implant sites.

What are the technical characteristics of the 17.010.02 elevator?

The flohr root elevator is distinguished by its technical reference 17.010.02. It features a Flohr-type active end, characterized by a specific curved shape (figure 2) that optimizes the leverage effect. The design of the shank and the tip is developed by Helmut Zepf to guarantee efficient force transmission while respecting the integrity of the surrounding tissues. Although exact dimensions are not specified, the Flohr range is recognized for its tip fineness allowing precise insertion into the periodontal ligament. The finish of the instrument allows for a stable grip for the practitioner during the rotation or tilting maneuvers necessary for luxation.

What are the contraindications for the use of this curved dental elevator?

Contraindications for the use of the Flohr curved dental elevator are related to the general limits of manual exodontia. It must not be used if the practitioner risks damaging critical adjacent anatomical structures, such as the maxillary sinus or the inferior alveolar nerve, without sufficient visibility and control. Furthermore, the use of this instrument is contraindicated in patients presenting with uncontrolled general medical contraindications to oral surgery. Excessive pressure on a weakened alveolar wall or on an adjacent tooth serving as a fulcrum must be avoided to prevent any bone fracture or iatrogenic lesion.

What are the maintenance precautions for this non-resorbable instrument?

As a reusable surgical instrument, the Flohr dental root elevator requires a rigorous decontamination and sterilization protocol after each use. The instructions from the manufacturer Helmut Zepf Medizintechnik GmbH regarding manual or automatic cleaning and autoclave sterilization should be followed. Precautions include the use of non-corrosive cleaning agents to preserve the surface condition of the instrument. Regular inspection of the active tip and the curvature is recommended to ensure the absence of deformation or wear that could compromise the effectiveness of the surgical procedure or patient safety during extraction.

Who is the manufacturer and what standards are respected?

The instrument is manufactured by Helmut Zepf Medizintechnik GmbH, a recognized manufacturer in the field of dental and surgical instrumentation based in Germany. As a medical device intended for surgery, it is designed according to high-precision manufacturing standards. Although specific certifications such as CE marking or regulatory class are not detailed here, Helmut Zepf products generally comply with current European standards for reusable medical devices. Practitioners are invited to consult the instructions for use and official labeling provided with reference 17.010.02 to verify regulatory compliance and specific reprocessing instructions.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.