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

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

The Hyundai Bioland T-GEN collagen membrane is a Class III medical device specifically designed for oral surgery and dental implantology. This resorbable membrane is developed from porcine-derived collagen, offering a structure adapted to the requirements of tissue regeneration. It comes in a 20x30mm format, ideal for covering intermediate-sized bone defects. As a biological barrier, it isolates the graft site from the surrounding soft tissues, thus promoting optimal healing. This Hyundai Bioland product integrates perfectly into the therapeutic arsenal of practitioners seeking a reliable solution for the reconstruction of periodontal and peri-implant tissues.

What are the clinical indications for this collagen membrane?

The T-GEN resorbable collagen membrane is primarily indicated for guided tissue regeneration (GTR) and guided bone regeneration (GBR) procedures. In implantology, it is used to protect filling materials during alveolar ridge augmentation or the filling of peri-implant defects. Its use maintains the space necessary for the formation of new bone while preventing invasion by fast-growing epithelial cells. This porcine-derived collagen membrane is an essential tool for securing bone grafts and ensuring the stability of the reconstructed volume before the placement or loading of implants.

What are the technical characteristics of the T-GEN 20x30mm membrane?

The T-GEN membrane is distinguished by its mechanical properties and biocompatibility. Manufactured by Hyundai Bioland Co., Ltd, it has dimensions of 20x30mm, offering a generous protection surface for various clinical configurations. Its porcine-derived collagen composition gives it excellent affinity with human tissues, facilitating its handling during surgical placement. This Class III medical device is designed to be resorbable, which eliminates the need for a second surgical intervention for its removal. Its structure is optimized to serve as an effective barrier while allowing the fluid exchanges necessary for the revascularization of the operated site.

What are the contraindications for the use of this device?

The use of the Hyundai Bioland T-GEN resorbable collagen membrane is strictly reserved for qualified healthcare professionals. As with any device of porcine origin, it is contraindicated in patients with a known hypersensitivity or allergy to porcine collagen. It is imperative not to use the product if the packaging is damaged, in order to guarantee the sterility of the device. Furthermore, its application must be avoided in sites presenting an active untreated infection. Practitioners must carefully evaluate the patient's general health status and local risk factors before any implantation to prevent post-operative complications.

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

The T-GEN membrane is a resorbable device, meaning it is naturally degraded by the body over time. This resorption process avoids the trauma associated with a removal surgery. To guarantee therapeutic success, it is crucial to read the instructions carefully before use. The practitioner must ensure adequate fixation of the membrane to prevent any displacement during the initial healing phase. Premature exposure of the membrane to the oral cavity must be avoided, as this could accelerate its degradation and compromise the underlying bone regeneration. Compliance with aseptic protocols and suturing techniques is fundamental to maintaining the integrity of the collagen barrier.

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

The T-GEN collagen membrane is manufactured by Hyundai Bioland Co., Ltd, a recognized player in the field of biomaterials. This medical device is classified as Class III, which attests to its high level of regulatory compliance and safety for long-term invasive surgical use. The manufacturing process follows strict standards to guarantee the purity of the porcine-derived collagen used. Hyundai Bioland ensures that each membrane meets the quality requirements necessary for dental surgery and implantology. Professionals can refer to official documentation and sources such as Delynov to confirm technical specifications and usage protocols compliant with MDR requirements.

State of the art

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