Backey Perma Sharp tissue forceps straight 15cm
The Pince à tissus Backey Perma Sharp droite 15cm is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What are the Backey Perma Sharp straight 15cm tissue forceps?
The Backey Perma Sharp tissue forceps are a high-precision surgical instrument developed by the manufacturer Hu-Friedy. This device is distinguished by its straight design and its total length of 15cm, offering an optimal balance for interventions in the oral cavity. Belonging to the Perma Sharp range, it benefits from a rigorous finish intended for fine tissue manipulation. As a Class I medical device, these forceps are specifically developed to meet the requirements of dental surgeons and implantologists practicing complex oral surgery procedures. Its structure allows for a secure grip without compromising the integrity of the manipulated soft tissues.
What are the clinical indications for this instrument?
These perma sharp surgical forceps are primarily indicated in oral surgery protocols requiring high dexterity, particularly during guided bone regeneration (GBR) phases. It is used by practitioners to lift, hold, or stabilize soft tissue flaps as well as for positioning barrier membranes. Its use also extends to periodontology and implantology, where precise management of gingival tissues is crucial for the aesthetic and functional success of the intervention. The straight configuration of the Backey forceps facilitates direct access to surgical sites, allowing precise tactile control during bone exposure or site closure.
What are the technical characteristics of the Backey forceps?
The Backey forceps from Hu-Friedy present rigorous technical specifications adapted to the clinical environment. It measures precisely 15cm, a standard dimension that ensures an ergonomic grip for the surgeon while allowing access to the posterior areas of the arch. The integrated Perma Sharp technology guarantees consistent manufacturing quality and increased durability of the gripping surfaces. This instrument is classified as a Class I medical device according to current regulations. Its straight design is ideal for linear traction maneuvers and tissue stabilization, minimizing accidental slips during critical phases of implant or periodontal surgery.
What are the contraindications for the use of these forceps?
According to information provided by the manufacturer Hu-Friedy Mfg. Co., LLC, specific contraindications are not detailed beyond standard oral surgery protocols. However, the use of this instrument is strictly reserved for qualified healthcare professionals. It is imperative not to use the forceps outside of its intended use, namely the manipulation of soft tissues. Practitioners must carefully consult the instructions before use to ensure the suitability of the instrument with the patient's clinical condition. As with any medical-grade stainless steel instrument, a prior check for the absence of structural damage to the instrument is necessary before each intervention.
What are the maintenance precautions for this non-resorbable instrument?
As this is a metallic surgical instrument and not a suture, the concept of resorption does not apply. However, the longevity of the Hu-Friedy Perma Sharp forceps depends directly on compliance with sterilization and cleaning protocols. As a Class I device, it must be cleaned, disinfected, and sterilized according to the manufacturer's instructions before each use. It is recommended to use non-corrosive cleaning solutions to preserve the Perma Sharp finish. Particular attention must be paid to the joints and jaws of the forceps during the maintenance cycle to guarantee perfect functionality and prevent any cross-contamination between patients in the dental surgery office.
Who is the manufacturer and what standards are respected?
The Backey tissue forceps are manufactured by Hu-Friedy Mfg. Co., LLC, a recognized company located in Chicago, USA. This medical device is listed under Class I, which attests to its compliance with basic regulatory requirements for manual surgical instruments. Hu-Friedy is a historic manufacturer in the dental field, guaranteeing that each instrument such as these perma sharp surgical forceps meets high production standards. Healthcare professionals must refer to the labeling and instructions for use provided by Hu-Friedy for any information relating to traceability and specific implementation protocols in a clinical setting.
State of the art
Guided bone regeneration (GBR) in implantology relies on membrane fixation quality.
Specifications
| Manufacturer | Hu-Friedy |
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