Collagen membrane 20x30mm resorbable for implantology T-GEN - Hyundai Bioland - Delynov

What is the Hyundai Bioland T-GEN resorbable collagen membrane?

The T-GEN membrane, developed by Hyundai Bioland, is a Class III medical device specifically designed for oral surgery and dental implantology procedures. It is a collagen membrane of porcine origin, developed to provide a resorbable structure adapted to the requirements of tissue regeneration. This product comes in a 20x30 mm format, offering a biological solution to separate soft tissues from bone tissues during the healing phase. As a resorbable device, it eliminates the need for a second surgical intervention for its removal, thus simplifying the clinical protocol for the practitioner and the patient. Its design by Hyundai Bioland Co., Ltd guarantees essential temporary structural support for the success of grafts.

What are the clinical indications for this device in oral surgery?

The T-GEN resorbable collagen membrane is exclusively indicated for guided tissue regeneration (GTR) and guided bone regeneration (GBR) procedures. In dental implantology, it serves as a protective barrier during the filling of bone defects, ridge augmentation, or alveolar preservation after extraction. Its primary role is to prevent the invasion of fast-growing epithelial and connective cells into the graft site, thereby allowing slower osteogenic cells to reconstruct the bone structure. This Hyundai Bioland device is an indispensable tool for securing the bone volumes necessary for the subsequent or simultaneous placement of dental implants, while promoting optimal biological integration into the oral environment.

What are the technical characteristics of the T-GEN 20x30 mm membrane?

The T-GEN membrane is distinguished by its mechanical and biological properties adapted to implantology. Manufactured from porcine-derived collagen by Hyundai Bioland Co., Ltd, it features dimensions of 20x30 mm, allowing it to cover intermediate to large surgical sites. Its resorbable nature is a major technical characteristic, as it is progressively degraded by the natural enzymatic processes of the human body. This device is categorized as Class III according to medical device regulations, which attests to its high level of requirement and safety for surgical implantation. Its handling is optimized for healthcare professionals, offering sufficient flexibility to adapt to the complex anatomical contours of the jaws while maintaining an effective barrier function.

What are the contraindications for the use of this collagen membrane?

The use of the Hyundai Bioland resorbable collagen membrane is subject to strict restrictions to ensure patient safety. It is contraindicated in individuals with a known hypersensitivity or allergy to porcine-derived collagen. Furthermore, like any implantable device, its use should be avoided in the presence of active infections at the surgical site or uncontrolled systemic pathologies that could compromise tissue healing or bone metabolism. It is imperative that the practitioner assesses the patient's general health status before the intervention. The use of this device is strictly reserved for healthcare professionals qualified in dental surgery and implantology, and a careful reading of the instructions for use is mandatory before any clinical handling.

How does resorption occur and what are the precautions for use?

The T-GEN membrane is designed to be resorbable, meaning it undergoes natural degradation in vivo without requiring manual removal. The resorption process maintains the barrier function during the critical period of bone regeneration before being fully integrated or eliminated by the surrounding tissues. To ensure the effectiveness of the device, the professional must ensure precise application and adequate fixation if necessary. A major precaution consists of avoiding premature exposure of the membrane to the oral environment, as wound dehiscence could accelerate collagen degradation by bacteria and compromise the result of the guided bone regeneration. Compliance with aseptic protocols and the recommendations of the manufacturer Hyundai Bioland is crucial for therapeutic success.

Who is the manufacturer and what standards are met by this product?

The T-GEN resorbable collagen membrane is manufactured by Hyundai Bioland Co., Ltd, a company specializing in biotechnological solutions. This medical device complies with strict regulatory requirements and benefits from a Class III classification, which corresponds to implantable medical devices presenting the highest risk and requiring an in-depth clinical evaluation. The manufacturer ensures the traceability and quality of the porcine-derived collagen used in the composition. As a product distributed by Delynov, it meets the safety standards required for dental surgery and implantology. Healthcare professionals must systematically refer to the technical instructions provided by Hyundai Bioland to ensure the conformity of use procedures and compliance with recommended storage conditions.

State of the art

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