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

What is the T-GEN 20x30 mm collagen membrane?

The T-GEN 20x30 mm collagen membrane, manufactured by Hyundai Bioland, is a Class III medical device specifically designed for implantology and oral surgery. It is a resorbable dental membrane developed from collagen of porcine origin. Its structure is optimized to serve as a protective barrier during bone healing phases. As a 20x30 collagen membrane, it offers a working surface suitable for intermediate-sized bone defects, allowing precise handling by the practitioner. This Hyundai Bioland Co., Ltd product meets the rigorous requirements for resorbable implantable devices used in dental practices and hospital settings.

What are the clinical indications for this Hyundai Bioland membrane?

This implanto collagen membrane is exclusively indicated for guided tissue regeneration (GTR) and guided bone regeneration (GBR) procedures. Its primary use in implantology consists of protecting the bone grafting site, thus preventing the invasion of fast-growing epithelial and connective cells, which allows osteogenic cells to reconstruct the alveolar volume. It is particularly recommended during immediate implant placement, sinus lifts, or the treatment of periodontal defects. The use of the Hyundai Bioland resorbable gbr membrane ensures the maintenance of the space necessary for osseointegration and graft stabilization.

What are the technical characteristics of the T-GEN membrane?

The T-GEN membrane is distinguished by its biological properties related to its porcine origin. With dimensions of 20x30 mm, it effectively covers standard surgical sites in implantology. As a Class III device, it is subject to strict biocompatibility controls. Its design allows for harmonious integration with surrounding tissues while maintaining its barrier function during the critical regeneration period. The Hyundai Bioland 20x30 collagen membrane is delivered sterile and ready to use for healthcare professionals, guaranteeing optimal safety during the surgical procedure.

What are the contraindications for the use of this device?

Although the source data does not list specific medical contraindications, the use of this collagen membrane of porcine origin requires a rigorous preoperative evaluation. Like any Class III implantable medical device, its use is reserved for qualified healthcare professionals. It is imperative to read the instructions carefully before use to check for any warnings related to the patient's systemic state or known sensitivities to components of porcine origin. Compliance with aseptic protocols and guided bone regeneration surgical techniques is essential to limit the risk of post-operative complications.

How does resorption occur and what are the precautions?

The T-GEN implantology collagen membrane is entirely resorbable, which eliminates the need for a second surgical intervention for its removal. The resorption process occurs naturally via enzymatic pathways. To guarantee regeneration success, the membrane must be correctly positioned and stabilized over the bone defect. The practitioner must ensure hermetic closure of the soft tissues to avoid any early exposure of the membrane to the oral environment, which could accelerate its degradation and compromise bone regeneration. Careful handling is required to maintain the integrity of the barrier for the entire duration necessary for osteogenesis.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hyundai Bioland Co., Ltd. This product is regulatorily classified as a Class III medical device, which corresponds to the highest level of control for implantable health products. Manufacturing by Hyundai Bioland follows strict protocols to guarantee the purity of the porcine collagen and the sterility of the final product. The use of this membrane is strictly reserved for healthcare professionals trained in oral surgery techniques. Compliance with the indications provided by Hyundai Bioland and systematic consultation of the technical instructions are essential to ensure the conformity of the medical act and patient safety.

State of the art

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