Resorbable collagen membrane 15X20 mm T-GEN - Hyundai Bioland - Delynov

What is the T-GEN 15X20 mm membrane?

The T-GEN 15X20 mm resorbable collagen membrane is a medical device designed by Hyundai Bioland for oral reconstructive surgery. It is a resorbable biological barrier intended to separate gingival tissues from the bone regeneration area. Its structure is specifically developed to maintain the space necessary for osteogenesis while being totally biocompatible. Offered by the manufacturer Hyundai Bioland Co., Ltd, this dental surgery collagen membrane avoids a second surgical intervention for its removal, as it is naturally degraded by the body. Its dimensions of 15X20 mm make it particularly suitable for targeted interventions requiring precise protection of the surgical site.

What are the clinical indications?

The purchase of a T-GEN dental resorbable membrane is indicated for various guided bone regeneration (GBR) and guided tissue regeneration (GTR) procedures. In clinical practice, it is used to cover bone defects after extraction, during ridge augmentation, or for sinus lift protection. It serves as a protective barrier over bone substitutes, preventing the migration of fast-growing epithelial and connective cells toward the graft site. This Hyundai Bioland device is therefore a key tool for securing the integration of grafts and promoting bone healing in complex implant and periodontal treatments.

What are the technical characteristics?

The T-GEN 15x20 collagen membrane is distinguished by its mechanical properties and ease of handling. With dimensions of 15 mm by 20 mm, it offers an ideal coverage surface for extraction sockets or sinus access windows. Its design by Hyundai Bioland ensures good tear resistance during handling and fixation, while maintaining sufficient flexibility to adapt perfectly to the anatomy of the surgical site. This surgical resorbable membrane features an optimized structure to ensure its barrier function during the critical regeneration phase, while allowing the nutritional exchanges necessary for the vitality of the underlying tissues.

What are the contraindications for use?

The use of the T-GEN periodontology collagen membrane should be avoided in patients with known hypersensitivities to collagen-derived products. It should not be applied to sites with an untreated active infection or severe inflammation. As with any regeneration device, insufficient vascularization of the recipient site or uncontrolled systemic pathologies (such as certain metabolic or immune disorders) can compromise the success of the intervention. It is the practitioner's responsibility to evaluate the patient's general health status and ensure the absence of specific contraindications mentioned in the technical instructions provided by the manufacturer Hyundai Bioland Co., Ltd before any implantation.

How does resorption occur and what are the precautions?

The T-GEN membrane is a resorbable device, meaning it undergoes progressive enzymatic degradation within the tissues. This natural elimination process avoids the trauma of a removal surgery. To guarantee optimal resorption and the success of the regeneration, the membrane must be completely covered by soft tissues during site closure, thus avoiding any early exposure to the oral environment which could lead to accelerated degradation or infection. The practitioner must ensure tension-free suturing to maintain the integrity of the barrier for the entire duration necessary for new bone tissue formation, in accordance with standard clinical protocols for Hyundai Bioland membranes.

Who is the manufacturer and what standards are respected?

The T-GEN device is manufactured by Hyundai Bioland Co., Ltd, a recognized manufacturer in the field of biomaterials for oral surgery. Production follows rigorous processes to guarantee collagen purity and the biological safety of the finished product. Although specific certification details are not listed here, the product is distributed by Delynov to meet the requirements of healthcare professionals. For any precise information regarding regulatory marking, device class, or specific manufacturing standards, surgeons are invited to systematically refer to the original labeling and the user manual accompanying each Hyundai Bioland membrane.

State of the art

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