Periodontal Probe #17-screw-in Colorvue handle #6

What is the Colorvue #17-non-threaded Periodontal Probe with #6 handle?

The Colorvue #17-non-threaded Periodontal Probe with #6 handle is a periodontal diagnostic instrument distributed by the brand Hu-Friedy. This device consists of an ergonomic #6 type handle and a specific Colorvue working end. Unlike traditional metal probes, the Colorvue system uses color codes to simplify the reading of clinical measurements. This particular model is designed without threads for end assembly, ensuring a stable configuration for soft tissue examination. As a Class I medical device, it meets the basic requirements for non-invasive instruments used in dental practices for the evaluation of gingival and periodontal health.

What are the clinical indications?

Clinical indications for this instrument from the brand Hu-Friedy primarily concern the evaluation of the health of the tooth's supporting tissues. It is used for measuring the depth of the sulcus or periodontal pockets, detecting gingival recessions, and evaluating the attachment level. In implant surgery and periodontology, it allows for monitoring the evolution of peri-implant tissues or the tissue response after root planing treatment. Its use is strictly reserved for qualified healthcare professionals, in accordance with the directives of the manufacturer Hu-friedy located in Chicago, USA. The instrument is essential for establishing an accurate periodontal diagnosis before any oral surgery or guided bone regeneration (GBR) intervention.

What are the technical characteristics?

The Colorvue #17-non-threaded Periodontal Probe is distinguished by its #6 handle, a standard diameter favoring a controlled grip during intra-oral handling. The Colorvue tip is designed to offer high visual contrast, which reduces the practitioner's eye fatigue during repeated measurements. The non-threaded design guarantees the integrity of the assembly during clinical use. This device is manufactured under the supervision of the manufacturer Hu-friedy. Classified as Class I, this instrument is reusable after following an appropriate sterilization protocol, although Colorvue tips may have specific life cycles according to the maintenance recommendations provided in the instructions for use attached to the Hu-Friedy brand product.

What are the contraindications for use?

According to information provided by the manufacturer Hu-friedy, specific contraindications are not exhaustively listed beyond standard warnings related to professional use. However, the use of this instrument is contraindicated in patients presenting extreme sensitivity of unanesthetized gingival tissues if the pressure exerted exceeds tolerance thresholds, or in situations where the integrity of the Colorvue tip is compromised. It is imperative not to use the instrument if signs of degradation, abnormal bending, or discoloration of markings are visible, as this could bias the clinical diagnosis. Compliance with asepsis protocols is mandatory to prevent any risk of cross-contamination.

What are the maintenance and durability precautions?

As a Class I non-resorbable instrument, the durability of the Colorvue #17-non-threaded Periodontal Probe depends directly on compliance with cleaning and sterilization cycles. It is recommended to clean the instrument immediately after use to avoid the fixation of organic debris. Although the #6 handle is designed to withstand standard autoclave sterilization methods, particular attention must be paid to the Colorvue tip to preserve the readability of the colored graduations. The manufacturer Hu-friedy recommends a systematic visual inspection before each intervention. Any marked wear of the tip must lead to the replacement of the instrument to guarantee the accuracy of the periodontal measurements essential for patient follow-up.

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 complies with regulatory requirements relating to Class I medical devices. This classification concerns low-risk instruments, primarily used for diagnosis or non-invasive treatment. The manufacturer emphasizes that the use of this instrument is strictly reserved for healthcare professionals. Before any use, it is essential to carefully read the instructions for use provided to ensure compliance with implementation and reprocessing procedures. Respect for these standards guarantees patient safety and the reliability of clinical results obtained in the practice.

State of the art

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