LUXA straight surgical elevator, 3mm working tip - Helmut Zepf (17.007.06TI) - Delynov

What is the LUXA straight surgical luxator?

The LUXA straight surgical luxator is an exodontia instrument designed by the manufacturer Helmut Zepf Medizintechnik GmbH. This device is distinguished by its rigid structure and its 3 mm wide straight working tip. It is specifically developed for oral surgery interventions requiring precise manipulation of periodontal structures. Unlike standard elevators, this LUXA model (reference 17.007.06TI) is optimized to penetrate the periodontal space. Its configuration allows the practitioner to exert controlled pressure to facilitate the luxation of the tooth or root. Helmut Zepf manufacturing quality guarantees an instrument adapted to the requirements of the surgical clinical environment.

What are the clinical indications for this instrument?

This surgical dental luxator is indicated for the initial mobilization of teeth during simple or complex extractions. It is particularly used in implant and oral surgery to sever the alveolar-dental ligament. Its 3 mm tip is adapted to the anatomical dimensions of common dental roots, allowing efficient insertion into the sulcus. The main clinical use consists of creating a space between the root and the alveolar bone in order to reduce the forces required for final avulsion. It is also suitable for root separation during hemisection or for the extraction of fractured root fragments. The use of this Helmut Zepf instrument contributes to the preservation of the alveolar bone plates.

What are the technical characteristics of model 17.007.06TI?

The surgical luxator referenced under code 17.007.06TI features precise technical specifications to meet the needs of dental surgeons. It has a 3 mm wide straight working tip, an ideal dimension for the majority of surgical sites in the anterior or posterior zone. The design of the active part is studied to ensure smooth insertion into the ligament space. Although specific material details are not provided in the raw technical data sheet, instruments in the Helmut Zepf range are recognized for their mechanical strength. The geometry of the instrument allows for optimal transmission of manual force without compromising the tactile sensitivity required during luxation.

What are the contraindications for the use of this luxator?

Contraindications for the use of this surgical luxator include clinical situations where excessive leverage could damage adjacent anatomical structures, such as the maxillary sinus or the mandibular canal. It must not be used as a blunt force lever, as its fine 3 mm tip is intended for ligament sectioning and not for massive elevation. As with any metallic instrument, a known hypersensitivity to the alloy components (not specified here) may constitute a contraindication. It is the practitioner's responsibility to evaluate bone density and root condition before application. Use on patients with bone healing disorders must be carried out with increased vigilance.

What are the maintenance and durability precautions?

To maintain the performance of this Helmut Zepf luxator, it is imperative to follow standard sterilization and cleaning protocols in force in dental practices. Although this product is non-resorbable and intended for repeated use after reprocessing, the integrity of the 3 mm tip must be checked before each intervention. Any deformation, dullness, or sign of corrosion must lead to the replacement of the instrument to guarantee patient safety and the effectiveness of the surgical gesture. It is recommended to use non-corrosive cleaning solutions and to respect autoclave cycles. Adequate storage in a dry environment preserves the mechanical properties of the surgical steel used by Helmut Zepf Medizintechnik GmbH.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Helmut Zepf Medizintechnik GmbH, a recognized player in the production of high-quality dental surgical instrumentation. Regarding standards and certifications, the regulatory class and specific CE marking are not mentioned in the current technical data for this product (reference 17.007.06TI). However, as a medical device manufacturer operating on the European market, Helmut Zepf is required to comply with general safety and performance requirements. Practitioners are invited to consult the instructions for use provided by the manufacturer or to contact Delynov to obtain up-to-date certificates of conformity and specific instructions relating to the Medical Device Regulation (MDR).

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