Periodontal probe Goldman-Fox no. 23 with handle no. 6 - Hu-Friedy - Delynov

What is the Goldman-Fox #23 periodontal probe?

The Goldman-Fox #23 periodontal probe is a manual diagnostic instrument designed by the recognized manufacturer Hu-Friedy. This device consists of a graduated working end and a #6 handle. It is specifically developed for oral health professionals performing periodontal examinations. Its structure allows for fine exploration of the tooth's supporting tissues. As a measurement instrument, it helps quantify the space between the gum and the tooth, providing essential data for monitoring patients' periodontal health. Its design meets the quality requirements of Hu-Friedy Mfg. Co., LLC, ensuring reliability during daily diagnostic procedures in dental surgery or periodontology practices.

What are the clinical indications for this probe?

The goldman fox probe is indicated for the systematic clinical evaluation of the periodontium. It is used by the practitioner to measure the depth of the sulcus or pathological periodontal pockets. This instrument is essential during the initial assessment, allowing for the determination of the level of attachment loss and tracking the progression of periodontal diseases over time. In implant and oral surgery, it can also be used to verify biological dimensions and soft tissue thickness. The use of this probe allows for precise documentation of the gingival status, thus facilitating the establishment of an appropriate treatment plan. It is exclusively reserved for professional use by qualified practitioners, in accordance with the instructions provided by Hu-Friedy.

What are the technical characteristics of the instrument?

This periodontal probe is distinguished by its precise millimeter graduations. The Goldman-Fox #23 model features specific markings according to the 10-9-8-7-5-3-2-1 sequence, allowing for direct and rapid reading of measured depths. It is equipped with a #6 type handle, offering a grip adapted to the requirements of meticulous clinical examinations. The thinness of the working tip is designed to penetrate the gingival sulcus without causing unnecessary tissue damage, while transmitting a precise tactile sensation to the clinician. Manufactured by Hu-Friedy Mfg. Co., LLC, this probe benefits from the brand's expertise in designing high-precision manual instruments for periodontics and oral surgery.

What are the contraindications for the use of this device?

According to the information provided by the manufacturer Hu-Friedy, the use of this instrument is strictly reserved for qualified health professionals. Specific contraindications are not detailed in the raw technical documentation, but the use of the instrument should be avoided if the patient presents extreme sensitivities or acute inflammations that do not allow for risk-free insertion. It is imperative to read the instructions for use carefully before any intervention. The practitioner must evaluate the patient's clinical condition to determine if periodontal exploration using a metallic probe is appropriate. Compliance with sterilization and asepsis protocols is mandatory between each patient to prevent any risk of cross-contamination.

What are the maintenance and handling precautions?

As a non-absorbable Class I instrument, the Goldman-Fox periodontal probe requires rigorous maintenance to maintain its measurement performance. After each use, the instrument must be cleaned, decontaminated, and sterilized in accordance with Hu-Friedy guidelines and current hygiene standards. Care must be taken not to alter the graduations during cleaning to ensure the accuracy of future measurements. Regular inspection of the probe tip is recommended to ensure the absence of bending or dullness that could distort clinical results. Handling must be performed with care to preserve the integrity of the instrument and ensure patient safety during exploration of the gingival sulcus.

Who is the manufacturer and what standards are respected?

The Goldman-Fox #23 periodontal probe is manufactured by Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This medical device is classified as Class I according to current regulations. As a recognized manufacturer in the dental sector, Hu-Friedy respects strict manufacturing standards to guarantee the compliance of its instruments. The product is intended exclusively for trained health professionals. Although specific CE marking is not mentioned in the source data, the instrument meets the regulatory requirements applicable to medical devices of its class. Compliance with the manufacturer's indications and warnings, as mentioned on the labeling, is essential to ensure safe and effective use in a clinical setting.

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