Instrument with composite handle number 6S XTS medium - Hu-Friedy - Delynov

What is the #6S XTS medium handle composite instrument?

The #6S XTS medium handle composite instrument is a manual tool designed by Hu-Friedy for practitioners specializing in aesthetic restorations. This device consists of a working part specific to the XTS range (Aluminum Titanium Nitride), optimized to minimize the adhesion of composite resins during handling. The #6S handle offers a grip adapted to the requirements of conservative surgery. As a medium composite instrument, it is positioned as a central element of the clinical arsenal for modeling direct restorative materials, guaranteeing a fluid application and a work structure consistent with Hu-Friedy brand standards.

What are the clinical indications for this composite restoration spatula?

This composite restoration spatula is indicated for all phases of shaping composite resins in dentistry. It is particularly useful for inserting material into Class I, II, III, IV, and V cavities, as well as for modeling occlusal and proximal surfaces. In restorative dental surgery, the instrument allows for sculpting dental anatomy with precision before polymerization. Its use is strictly reserved for qualified healthcare professionals involved in conservative care protocols or complex aesthetic rehabilitations requiring rigorous handling of biomaterials.

What are the technical characteristics of this Hu-Friedy instrument?

The Hu-Friedy instrument is distinguished by its technical design focused on clinical performance. Equipped with a #6S type handle, it ensures optimal balance during the modeling phases. The XTS technology integrated into the working part is specifically developed to provide a dark surface contrasting with composite shades, while significantly reducing the sticking of the material to the instrument. This xts composite spatula is classified as a Class I medical device according to current regulations. Its manufacture by Hu-Friedy Mfg. Co., LLC follows strict quality protocols to meet the requirements of dental practices and oral surgery centers.

What are the contraindications for the use of this device?

According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not listed beyond the intended use. However, the use of this instrument is strictly reserved for duly trained healthcare professionals. The instrument should not be used outside of its indications for modeling and applying composites. Any misuse could compromise the integrity of the device or the clinical outcome. Practitioners must systematically refer to the instructions for use and manufacturer warnings located in Chicago, USA, to ensure patient safety and the longevity of the instrumentation.

What are the maintenance and handling precautions?

Although the instrument is not an absorbable suture, it requires rigorous maintenance precautions. As a Class I medical device, it must be cleaned, disinfected, and sterilized before each use in accordance with current clinical protocols. It is imperative to read the instructions carefully before any handling. Preservation of the XTS coating is essential to maintain the anti-adherent properties of the spatula. Professionals must inspect the instrument before use to detect any signs of wear or degradation of the working surface, in order to ensure flawless composite modeling and optimal safety during care.

Who is the manufacturer and what standards are respected?

The official manufacturer of this instrument is Hu-Friedy Mfg. Co., LLC, headquartered at 3232 N. Rockwell St. Chicago, Il 60618, USA. This medical device is listed under Class I. The Hu-Friedy brand is internationally recognized for the quality of its precision instruments in dental surgery. Compliance with American and international manufacturing standards ensures practitioners a reliable tool for their daily interventions. In accordance with MDR regulations, this product is exclusively reserved for healthcare professionals. Each user must ensure compliance with the indications and warnings provided by the manufacturer for practice that meets regulatory requirements.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.