Vis hexagonale 678-206/303. 1 pce - Hu-Friedy

What is the Hu-Friedy hex screw 678-206 + 678-303?

The hex screw 678-206 + 678-303, offered by the brand Hu-Friedy, is a precision medical device designed for oral surgery interventions. Packaged individually (1 pce), this technical reference falls within the category of Guided Bone Regeneration (GBR) products. Manufactured by Hu-Friedy Mfg. Co., LLC, it meets the rigorous quality requirements imposed on surgical instruments. This product is specifically developed to meet the needs of practitioners during complex procedures requiring reliable fixation and ergonomic handling thanks to its hexagonal head.

What are the clinical indications for this device?

This Hu-Friedy device is indicated for dental and implant surgery procedures, particularly within the framework of guided bone regeneration (GBR). Its use is strictly reserved for qualified healthcare professionals. It is used during surgical protocols requiring the use of specific fixation screws to stabilize regeneration devices. Precise indications must be determined by the dental surgeon or oral surgeon based on the patient's clinical needs and the chosen operative protocol, while respecting the warnings provided by the manufacturer Hu-Friedy Mfg. Co., LLC.

What are the technical characteristics of this hex screw?

The hex screw 678-206 + 678-303 is distinguished by its robust design adapted to the requirements of the oral environment. Although exact dimensional specifications or materials are not detailed in the provided technical documentation, its dual reference (678-206 and 678-303) indicates a coherent functional set for GBR fixation systems. As a product of the Hu-Friedy range, it benefits from the expertise of Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA. This device is classified as a Class I instrument, guaranteeing a compliant manufacturing standard for non-invasive or low-risk surgical tools.

What are the contraindications for the use of this product?

Contraindications for the use of the Hu-Friedy hex screw include any situation where oral surgery itself is contraindicated for the patient (serious systemic health problems, uncontrolled bleeding disorders). Furthermore, the use of this device is contraindicated outside of a professional setting, as its use is exclusively reserved for healthcare practitioners. It is imperative not to use this product if the integrity of the packaging is compromised or if clinical conditions do not allow for adequate stabilization of the regeneration material. The practitioner must systematically refer to the instructions for use before any intervention.

What are the precautions for use and handling?

To ensure patient safety and the effectiveness of the intervention, several precautions must be observed with this Hu-Friedy device. The manufacturer emphasizes the importance of carefully reading the instructions before use. Handling must be performed with instruments compatible with the hexagonal profile of the screw to avoid any technical damage. As a Class I device, it must be processed according to the sterilization and hygiene protocols in force in dental offices and operating rooms. The warnings from the manufacturer Hu-friedy 3232 N. Rockwell St. Chicago, Il 60618 USA must be scrupulously followed to prevent any risk of intraoperative complications.

Who is the manufacturer and what standards are respected?

The device is manufactured by Hu-Friedy Mfg. Co., LLC, located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This product is classified under Class I according to medical device regulations. The Hu-Friedy brand is globally recognized for its commitment to the quality and precision of dental instruments. Compliance with the manufacturer's indications and warnings is essential to ensure the conformity of clinical use. Although specific CE marking is not mentioned in the source data, the Class I classification confirms that the device meets the safety and performance standards applicable to its category for use by healthcare professionals.

State of the art

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