Modified McCall Turgeon curette #17/18S handle #6

What is the modified McCall Turgeon curette #17/18S handle #6?

The modified McCall Turgeon curette #17/18S is a precision manual instrument developed by the manufacturer Hu-friedy for the brand Hu-Friedy. This device, belonging to the INSTRU category, is specifically configured with a #6 handle to offer a grip adapted to the requirements of periodontology. As a periodontics curette, its structure is optimized to access complex clinical zones. This medical device is classified as a Class I instrument, meeting rigorous manufacturing standards for repeated use after sterilization in a clinical setting. Its modified design allows it to meet specific needs for curettage and cleaning of root surfaces during periodontal care.

What are the clinical indications for this instrument?

The intended use of this periodontics curette from the brand Hu-Friedy primarily concerns the treatment of periodontal diseases. It is indicated for deep scaling and root planing. Practitioners use the modified McCall Turgeon #17/18S to mechanically remove subgingival calculus and bacterial bio-film accumulated in periodontal pockets. It is also employed for the removal of granulation tissue during flap surgery or gingival curettage. Its use is strictly reserved for qualified healthcare professionals, such as dental surgeons and periodontists, within the framework of therapeutic protocols aimed at restoring the health of the tooth's supporting tissues.

What are the technical characteristics of this instrument?

The modified McCall Turgeon curette #17/18S is distinguished by its specific technical configuration under the handle reference #6. Manufactured by the manufacturer Hu-friedy for Hu-Friedy, it features working ends designed for optimal cutting efficiency during periodontal debridement. As a Class I device, it is designed to withstand the decontamination and sterilization cycles required in a dental office. The geometry of the #17/18S working part is adapted to reach precise anatomical zones, facilitating passage in interproximal spaces and along roots. The #6 handle is selected for its diameter and texture, allowing for the tactile control necessary during curettage maneuvers requiring controlled force.

What are the contraindications for the use of this curette?

According to the information provided by the manufacturer Hu-friedy, specific contraindications are not listed exhaustively beyond general warnings. However, the use of this instrument from the brand Hu-Friedy is strictly reserved for trained healthcare professionals. Inappropriate use by unqualified personnel constitutes a major contraindication. Furthermore, as with any periodontics curette, its use may be contraindicated on dental surfaces presenting unmanaged extreme hypersensitivity or on fragile prosthetic restorations that could be damaged by the mechanical action of the steel. The instructions for use should be systematically referred to before any intervention to ensure patient safety.

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

As a reusable Class I surgical instrument and not an absorbable device, the modified McCall Turgeon curette #17/18S requires a rigorous maintenance protocol. After each use in surgery or periodontics care, the instrument must be cleaned, disinfected, and sterilized in accordance with the instructions from the manufacturer Hu-friedy located in Chicago, USA. Professionals must regularly inspect the condition of the cutting edges of the periodontics curette to maintain its clinical effectiveness. Periodic sharpening may be necessary, while respecting the original morphology of the #17/18S tip. Compliance with these precautions ensures the longevity of the Hu-Friedy instrument and prevents the risks of cross-contamination between patients.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is marketed under the brand Hu-Friedy and benefits from a Class I regulatory classification. This classification indicates that the instrument meets the safety and performance requirements defined for manual non-invasive or invasive medical devices for temporary use. In accordance with the Medical Device Regulation (MDR), this instrument is reserved exclusively for professional use. The manufacturer emphasizes the importance of carefully reading the manual before use to ensure compliance with the safety and hygiene protocols in force in the European Union and internationally.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.