Williams Periodontal Probe #23-screw-thread Colorvue handle #6

What is the Williams #23-screw-thread Colorvue periodontal probe handle #6?

The Williams #23-screw-thread Colorvue periodontal probe is a specialized diagnostic instrument distributed under the brand Hu-Friedy. This device consists of an ergonomic #6 type handle and a specific measuring tip using the Colorvue system. Unlike traditional metal probes, this model integrates a colored marking system for easier reading of millimeters. The screw-thread structure allows the tip to be securely fixed to the handle, ensuring optimal tactile transmission during exploration of the sulcus or periodontal pockets. This product from the brand Hu-Friedy is designed to meet the precision requirements of dental surgeons and periodontists.

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

The use of the Williams #23 Colorvue probe from the brand Hu-Friedy is indicated for the systematic evaluation of periodontal health. It allows for measuring pocket probing depth, detecting bleeding on probing, and evaluating gingival recessions. In implant surgery, it is used to check the height of keratinized tissue and peri-implant depth. Williams graduations are a standard for quantifying attachment loss. This device is exclusively reserved for healthcare professionals trained in periodontal diagnostic techniques, in accordance with the directives of the manufacturer Hu-friedy based in Chicago, USA.

What are the technical characteristics of the probe and handle?

This probe is distinguished by its #6 handle, offering a diameter designed to reduce hand fatigue during prolonged examinations. The technical specificity lies in its Williams tip equipped with the Colorvue system, which features marked visual contrasts for rapid identification of measurements. The screw-thread fixation mechanism ensures a rigid connection between the tip and the handle, avoiding any mechanical play during insertion into the marginal periodontium. Manufactured by Hu-friedy, this instrument belongs to the GBR (Guided Bone Regeneration) category within the catalog, although its primary function is precise clinical diagnosis before any surgical intervention.

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 healthcare professionals. There are no specific medical contraindications listed other than those related to standard periodontal examination protocols. However, the instrument should not be used if the screw thread is damaged or if the Colorvue tip shows wear on the markings, which could bias the clinical diagnosis. Practitioners must refer to the instructions for use before any manipulation to ensure patient safety and the integrity of the equipment from the brand Hu-Friedy.

What are the maintenance precautions for this non-resorbable probe?

As a non-resorbable diagnostic instrument, the Williams #23 probe from the brand Hu-Friedy requires a rigorous sterilization and disinfection protocol between each patient. Although material details are not specified, maintenance of the screw thread is crucial to ensure the durability of the assembly between the #6 handle and the Colorvue tip. It is imperative to follow the cleaning recommendations from the manufacturer Hu-friedy to avoid any corrosion or degradation of the colored markings. Regular visual inspection of the Williams graduations is advised to maintain constant measurement accuracy during clinical assessments.

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 classified as a Class I medical device, meeting the basic regulatory requirements for non-invasive diagnostic instruments. The brand Hu-Friedy ensures the distribution of this precision tool. It is reminded that the use of this probe is strictly reserved for healthcare professionals. Compliance with Class I ensures that the instrument has undergone the necessary conformity checks for its application in dental offices and surgical environments.

State of the art

Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.