Kit for Lateral Sinus Approach (KALS) (HLRSNK) by OSSTEM - DELYNOV

What is the Osstem Lateral Approach Sinus Kit (KALS)?

The Lateral Approach Sinus Kit, referenced under the code KALS by Osstem, is a set of surgical instruments specifically configured for oral surgery interventions. This sinus lift surgery kit groups together the tools necessary to approach the lateral wall of the maxillary sinus. Designed by the manufacturer Osstem Implant Co., Ltd, this set provides practitioners with a structured solution for the critical stages of bone opening. Its composition is designed to meet the requirements of modern implantology, offering a logical organization of instruments to optimize the workflow in the operating room during sinus augmentation procedures.

What are the clinical indications for this kit?

The lateral sinus approach kit is indicated for pre-implant surgery interventions requiring bone grafting in the posterior sector of the maxilla. It is mainly used when the residual bone height is insufficient for immediate implant placement. This device allows for the creation of a precise lateral window to access the sinus cavity, an essential preliminary step for the detachment of the Schneiderian membrane and the placement of bone substitutes. The use of this sinus approach kit is reserved for dental surgeons and stomatologists trained in vestibular sinus floor elevation techniques.

What are the technical characteristics of the HLRSNK kit?

The HLRSNK kit, or KALS from Osstem, is characterized by a selection of rotary and manual instruments adapted to the bone density of the maxilla. Although detailed material specifications are not explicitly listed, this type of sinus lift kit generally includes specific drills and cutting instruments designed to minimize thermal heating during the creation of the bone flap. The overall design aims to secure the sinus approach by allowing rigorous control of the drilling depth. Each component is arranged in an organized storage tray, facilitating cleaning and sterilization according to the protocols in force in dental practices.

What are the contraindications for the use of this device?

The contraindications for using the Osstem sinus approach kit are related to the general contraindications of sinus lift surgery. These include untreated acute or chronic sinus pathologies, such as maxillary sinusitis, polyps, or sinus tumors. Systemic contraindications may also apply, such as uncontrolled coagulation disorders or severe metabolic bone diseases. It is the practitioner's responsibility to evaluate the patient's general health status and verify the absence of local infections before undertaking surgery with this kit. A prior radiological analysis by CBCT is essential to identify any anatomical variants contraindicating the lateral approach.

What are the maintenance and storage precautions?

Like any implant surgery instrument, the elements of the Osstem KALS kit must be handled with care to preserve their cutting power and structural integrity. After each use, it is imperative to follow a protocol of decontamination, manual or ultrasonic cleaning, and autoclave sterilization in accordance with the instructions from the manufacturer Osstem Implant Co., Ltd. Instruments must be visually inspected before each intervention to detect any signs of wear or corrosion. Rigorous maintenance guarantees the longevity of the kit components and ensures the microbiological safety of the surgical acts performed.

Who is the manufacturer and what standards are respected?

The Lateral Approach Sinus Kit (KALS) is manufactured by Osstem Implant Co., Ltd, an internationally recognized manufacturer in the field of dental implantology. The production of these devices follows strict industrial manufacturing protocols. For precise information on the regulatory class, CE marking, or specific ISO certifications for this lot, users are invited to refer to the product labeling and the instructions for use provided by Osstem. As a medical device intended for invasive surgery, it must be used exclusively by qualified healthcare professionals, in compliance with good clinical practices and hospital hygiene standards.

State of the art

Single-use sterile surgical kits significantly reduce intraoperative contamination.