North-Carolina Periodontal Probe #23 handle #31 15-14-13....3-2-1

What is the North-Carolina #23 periodontal probe with #31 handle?

The North-Carolina #23 periodontal probe with #31 handle, marketed under the brand Hu-Friedy, is a manual diagnostic instrument designed for clinical evaluation of periodontal tissues. This device consists of a specific graduated rod and an ergonomic handle referenced #31. Its structure allows for delicate insertion into the gingival sulcus to measure the space between the gum and the tooth. Manufactured by the manufacturer Hu-Friedy, this probe meets the quality requirements necessary for routine examinations and complex surgical interventions. Hu-Friedy instrumentation is recognized for its reliability in the field of oral surgery and periodontology, offering a clear reading of the clinical measurements essential to the practitioner.

What are the clinical indications for this instrument?

In dental and periodontal surgery, the North-Carolina probe from the brand Hu-Friedy is indicated for the precise measurement of periodontal pocket depth, evaluation of clinical attachment level, and detection of gingival recession. It is also used to quantify gingival hyperplasia and verify tissue stability after implant surgery or a debridement flap. The continuous graduation from 1 to 15 mm allows for fine analysis of the morphology of bone defects and horizontal or vertical bone loss. Its use is paramount during the establishment of the initial periodontal diagnosis as well as for the regular monitoring of patients in the periodontal maintenance phase to detect any disease progression.

What are the technical characteristics of the North-Carolina #23 probe?

The North-Carolina #23 probe is distinguished by its millimeter graduation ranging from 1 to 15 mm (1-2-3-4-5-6-7-8-9-10-11-12-13-14-15). This technical specificity allows for increased precision compared to standard probes often limited to 3 mm increments. The #31 handle associated with this instrument from the brand Hu-Friedy offers a grip adapted to the requirements of daily practice. The working part is designed to glide without excessive trauma along the root surface. As a Class I device, this probe complies with the rigorous manufacturing standards imposed by the manufacturer Hu-Friedy, guaranteeing resistance to standard sterilization processes in dental offices while maintaining the legibility of the millimeter markings.

What are the contraindications for the use of this probe?

According to information provided by the manufacturer Hu-Friedy, the use of this instrument is reserved exclusively for qualified healthcare professionals. There are no absolute medical contraindications listed specifically for this Class I device, outside of clinical situations where the insertion of an instrument into the sulcus could aggravate an uncontrolled acute infection or cause unbearable pain for the patient without prior anesthesia. It is imperative to read the instructions carefully before use to become aware of all warnings. The practitioner must ensure the integrity of the probe before each use to avoid any risk of tissue injury related to a damaged or bent tip.

What are the maintenance and durability precautions?

Although this product is non-absorbable as it is metallic, its durability depends on compliance with cleaning, disinfection, and sterilization protocols. Like any instrument from the brand Hu-Friedy, the North-Carolina probe must be treated according to the manufacturer's recommendations to avoid corrosion or premature fading of the millimeter graduations. It is advisable to use neutral pH cleaning solutions and avoid overly aggressive chemical agents. Regular visual inspection of the graduated rod 15-14-13...3-2-1 is necessary to guarantee the accuracy of clinical measurements. Rigorous maintenance ensures not only patient safety but also the longevity of the instrumentation within the oral surgery technical platform.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hu-Friedy, located in Chicago, USA. This product is regulatorily classified as Class I, which corresponds to medical devices presenting a low degree of risk, in accordance with current regulations for manual dental instrumentation. Although specific CE marking is not mentioned in the source data, compliance with Class I attests to conformity with essential safety and performance requirements for diagnostic instruments. Traceability and manufacturing quality are ensured by the manufacturer, a globally recognized player in the dental sector. Professionals must refer to the instructions for use to guarantee use in accordance with professional standards.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.