Gracey curette #3/4 #6 AF handle labial/lingual
The Curette Gracey #3/4 manche #6 AF labial/lingual is a medical device manufactured by le fabricant.
- Compliance: Medical device Class I.
- Manufacturer: le fabricant.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the Gracey #3/4 handle #6 AF labial/lingual curette?
The Gracey #3/4 curette from the Hu-Friedy brand is a precision instrument belonging to the INSTRU category, specifically developed for periodontal instrumentation of anterior teeth. This After Five (AF) model is distinguished by a configuration adapted for difficult access, mounted on a number 6 handle. As a manual dental curette, it is designed to work on labial and lingual faces. This medical device is manufactured by the manufacturer Hu-Friedy, a recognized player in the field of surgical instrumentation. Its structure allows for a specific approach to tissues, guaranteeing handling adapted to the requirements of oral health professionals in a clinical environment.
What are the clinical indications?
The clinical indications for this instrument from the Hu-Friedy brand primarily concern non-surgical and surgical periodontal treatment. It is used for subgingival scaling and root planing of incisors and canines. Thanks to its After Five specificity, it allows reaching deep periodontal pocket areas where standard instruments might be limited. Its use is reserved for qualified health professionals, such as dental surgeons and periodontists, for the removal of calculus deposits and biofilm on labial and lingual root surfaces. The instrument is integrated into etiological periodontal therapy and maintenance protocols.
What are the technical characteristics?
The Gracey #3/4 After Five curette from the Hu-Friedy brand features precise geometric characteristics for work in anterior sectors. The #6 handle offers a specific grip for control of the gesture during planing. The After Five terminology indicates an adaptation of the shank to facilitate insertion into deep pockets. This device is classified as Class I according to medical device regulations. The design of the working part is optimized for labial and lingual surfaces, ensuring cutting efficiency on a single sharp edge, a characteristic specific to Gracey-type curettes. Manufacturing is carried out by Hu-Friedy in the USA.
What are the contraindications for use?
According to the information provided by the manufacturer Hu-Friedy, specific contraindications are not listed exhaustively beyond general safety warnings. However, the use of this instrument is strictly reserved for trained health professionals. Standard clinical protocols related to manual periodontal instrumentation must be respected. Particular attention must be paid to the state of the soft tissues and the integrity of the dental surfaces. As with any Class I instrument, it is imperative to read the instructions carefully before use to ensure the suitability of the device for the patient's clinical situation and to avoid any inappropriate use that could compromise treatment results.
What are the precautions for use and maintenance?
As a non-resorbable and reusable instrument, this manual dental curette requires rigorous management by the dental practice. Before each use, the practitioner must check the condition of the cutting edge and the integrity of the #6 handle. The sterilization and cleaning process must scrupulously follow the recommendations of the manufacturer Hu-Friedy to maintain the physical properties of the Class I instrument. Precautions include systematic verification of the absence of corrosion or deformation before insertion into the mouth. Compliance with asepsis protocols is fundamental to guarantee patient safety and the longevity of the instrumentation during interventions on labial and lingual surfaces.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-Friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is listed under the Hu-Friedy brand and belongs to Class I of medical devices. Compliance with regulatory standards is evidenced by the classification and indications of intended use (MDR). As a Class I instrument, it meets the safety and performance requirements defined for this category of manual surgical tools. Health professionals must refer to the instructions for use provided by the manufacturer for all technical and regulatory details applicable to this After Five curette.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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