Buser Periosteal Elevator, Black Line - Hu-Friedy - Delynov

What is the Buser Black Line periosteal elevator - Hu-Friedy?

The Buser periosteal elevator, from the Black Line range developed by Hu-Friedy, is a specialized surgical instrument used in dentistry for soft tissue management. This device is distinguished by its specific design adapted to the requirements of micro-surgery and modern implantology. Manufactured by Hu-Friedy Mfg. Co., LLC, this instrument belongs to the category of hand instruments (INSTRU) intended for the delicate manipulation of periodontal structures. Its structure allows for an optimal grip for technical gestures requiring great finesse. As a Class I device, it meets the basic regulatory requirements for non-invasive or temporary invasive instruments, thus guaranteeing a rigorous manufacturing standard for clinicians.

What are the clinical indications for this instrument?

The Buser elevator is primarily indicated for the elevation of full-thickness flaps during oral, periodontal, or implant surgeries. Its use is recommended for delicately separating the periosteum from the alveolar bone without lacerating the surrounding soft tissues. It is particularly useful in the initial phases of surgical site exposure, allowing the practitioner to obtain clear visibility of the surgical field. Surgeons also use it to maintain the flap in a retracted position during implant drilling or the placement of bone grafting materials. This instrument is reserved exclusively for healthcare professionals trained in these technical acts, in accordance with the directives provided by the manufacturer Hu-Friedy.

What are the technical characteristics of this device?

Technically, this Buser periosteal elevator is characterized by a double functional end allowing for versatility during the intervention. The Black Line series from Hu-Friedy often incorporates specific finishes to reduce reflections under operating lights and improve visual contrast with the tissues. Although exact dimensions are not specified here, the design is optimized for access to restricted anatomical areas. As a Class I instrument, it is designed to be reusable after an appropriate cleaning and sterilization cycle, scrupulously following hospital protocols and manufacturer instructions. Its structural robustness ensures a faithful transmission of the force applied by the surgeon during periosteal detachment.

What are the contraindications for the use of this elevator?

Specific contraindications mentioned by the manufacturer Hu-Friedy mainly concern use by unqualified persons, as this device is strictly reserved for healthcare professionals. From a clinical perspective, the use of this instrument is contraindicated if the soft tissues present uncontrolled acute inflammatory pathologies or if the patient's tissue fragility risks leading to major complications during detachment. The instrument should not be used for functions for which it is not intended, such as the elevation of tooth roots or the luxation of teeth, which could damage the working ends. The practitioner must always read the instructions carefully before use to ensure the adequacy between the patient's clinical status and the intended use of the device.

What are the maintenance and handling precautions?

As a non-resorbable and reusable instrument, precautions focus on maintaining the integrity of the instrument. After each oral surgery intervention, the Buser elevator must undergo a decontamination, manual or ultrasonic cleaning, and steam sterilization protocol. It is imperative to inspect the instrument before each use to detect any trace of corrosion, deformation, or wear of the active parts that could compromise patient safety. Careful handling is required to avoid dulling the active edges during storage. Compliance with the sterilization cycles recommended by Hu-Friedy Mfg. Co., LLC guarantees the longevity of the instrument and the microbiological safety essential in a surgical environment.

Who is the manufacturer and what standards are respected?

The Buser periosteal elevator is manufactured by Hu-Friedy Mfg. Co., LLC, with its headquarters located at 3232 N. Rockwell St. Chicago, Il 60618 USA. This manufacturer is globally recognized in the dental sector for the quality of its instruments. This product is classified as a Class I medical device according to current regulations. Although specific CE marking is not detailed in the source data, compliance with American and international manufacturing standards for Class I instruments is ensured by Hu-Friedy's quality control processes. Professionals must refer to the instructions for use and manufacturer warnings to guarantee use in accordance with the safety and performance requirements expected for this type of surgical instrumentation.

State of the art

Specialized surgical instrumentation is evolving towards ergonomic designs.