Williams #17 Periodontal Probe handle #6 1-2-3-5-7-8-9-10

What is the Williams #17 periodontal probe #6 handle 1-2-3-5-7-8-9-10?

The Williams #17 periodontal probe #6 handle 1-2-3-5-7-8-9-10 is a manual diagnostic instrument used in periodontology and oral surgery. Distributed under the brand Hu-Friedy, this probe is distinguished by its #6 type handle offering a grip adapted to prolonged clinical procedures. It features specific graduations according to the Williams pattern, namely 1, 2, 3, 5, 7, 8, 9, and 10 millimeters. The absence of 4 and 6 mm marks is characteristic of this model, helping to avoid certain confusions during rapid reading in a clinical setting. This instrument is a Class I medical device, designed to meet the requirements of practitioners for evaluating the health of the tooth's supporting tissues.

What are the clinical indications for this Hu-Friedy instrument?

The clinical indications for this periodontal probe from the brand Hu-Friedy primarily concern the quantitative and qualitative evaluation of the periodontal space. It is indicated for measuring periodontal pocket depth, evaluating clinical attachment loss, and monitoring gingival recession. In implant surgery, it allows for checking soft tissue thickness or site depth before abutment placement. The #17 explorer part is particularly useful for detecting subgingival calculus, examining furcation areas, and identifying root surface irregularities. Its use is strictly reserved for qualified healthcare professionals within the framework of comprehensive periodontal diagnostics or post-operative follow-ups.

What are the technical characteristics of the Williams #17 probe?

Technically, the Williams #17 probe is characterized by a working part calibrated with rigorous precision at intervals of 1-2-3-5-7-8-9-10 mm. These graduations are engraved to ensure optimal visibility during insertion into the sulcus. The #6 handle is designed to provide an adequate balance between weight and diameter, facilitating the tactile transmission necessary for detecting subgingival obstacles. Manufactured under the supervision of the manufacturer Hu-friedy, this instrument complies with the manufacturing standards for Class I medical devices. The combination of the Williams probe and the #17 explorer into a single instrument reduces the number of manipulations during initial diagnosis or periodontal maintenance phases.

What are the contraindications for the use of this probe?

According to information from the manufacturer Hu-friedy, the use of this instrument is reserved exclusively for healthcare professionals. There are no specific medical contraindications listed other than those related to standard periodontal examination protocols. However, the practitioner must exercise caution when examining highly inflammatory tissues or recently operated areas to avoid unnecessary trauma. It is imperative to read the instructions carefully before use to ensure compliance with sterilization and maintenance protocols. The instrument must not be used if signs of graduation degradation or tip bending are observed, in order to guarantee the reliability of clinical measurements.

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

As it is a manual metallic instrument and not an absorbable device, the usage precautions from the brand Hu-Friedy focus on maintaining the integrity of the graduations and the explorer tip. The device must be cleaned, disinfected, and sterilized before each use in accordance with the instructions from the manufacturer Hu-friedy located in Chicago, USA. It is recommended to use non-corrosive cleaning solutions to preserve the Williams millimeter markings. Regular visual inspection is necessary to check for the absence of corrosion or dulling of the #17 tip. Rigorous maintenance guarantees the accuracy of measurements from 1 to 10 mm and extends the operational life of the instrument in the dental office.

Who is the manufacturer and what standards are respected?

The official manufacturer of this Williams #17 probe is Hu-friedy, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This medical device is classified as Class I according to current regulations. As a product of the brand Hu-Friedy, it is subject to the manufacturer's rigorous quality controls to ensure compliance with safety and performance requirements for medical devices. Healthcare professionals must refer to the indications and warnings provided by Hu-friedy to ensure compliant use. Although specific CE marking is not mentioned in the source data, the Class I classification confirms its status as a regulated medical device intended for professional use in dental surgery and periodontology.

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