Resorbable collagen membrane 15X20 mm 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 implantology procedures. It is a resorbable collagen membrane of porcine origin, structured to provide an effective solution in tissue regeneration protocols. This device is available in a 15X20 mm format, suitable for interventions requiring a temporary biological barrier. As a high-tech biomedical product, the Hyundai Bioland membrane ensures a tissue separation function during the critical healing phase. Its use is strictly reserved for qualified healthcare professionals, guaranteeing an application that complies with the requirements of modern dental surgery.

What are the clinical indications for this regeneration device?

The Hyundai Bioland T-GEN resorbable collagen membrane is primarily indicated for guided tissue regeneration (GTR) and guided bone regeneration (GBR). In surgery and implantology, it serves to protect surgical sites by preventing the invasion of fast-growing soft tissues into bone defects, thus promoting optimal osteogenic reconstruction. It is used to cover extraction sites, protect filling materials, or stabilize the operative area. This Hyundai Bioland brand device meets the needs of practitioners seeking to secure their tissue reconstruction protocols thanks to a resorbable biological barrier of porcine origin, perfectly integrated into current clinical standards.

What are the technical characteristics of the T-GEN 15X20 mm membrane?

This medical device is distinguished by its intrinsic properties related to the porcine collagen selected by Hyundai Bioland Co., Ltd. With dimensions of 15X20 mm, this membrane offers a working surface adapted to localized defects in implantology. Its resorbable structure eliminates the need for a second surgical intervention for its removal, thereby simplifying post-operative follow-up for both the patient and the practitioner. Classified as Class III according to current regulations, it meets strict safety and performance requirements for implantable devices. Its design allows for precise handling during placement at the surgical site, ensuring effective and temporary protection during the guided tissue regeneration phase.

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

Although the provided sources do not list specific detailed contraindications, the use of the Hyundai Bioland T-GEN membrane is subject to standard implant surgery protocols. Like any porcine-derived collagen device, its use is contraindicated in patients with a known hypersensitivity or allergy to porcine proteins. It is the responsibility of the healthcare professional to assess the patient's clinical status before the intervention. Use is strictly reserved for trained practitioners. It is imperative to carefully read the instructions for use attached to the product before any application to identify any specific usage restrictions mentioned by the manufacturer Hyundai Bioland Co., Ltd.

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 without requiring manual explantation. This resorption process maintains the barrier function for the period necessary for guided tissue regeneration. To guarantee the effectiveness of the treatment, the practitioner must ensure rigorous aseptic handling. It is essential to follow the indications for protecting surgical sites to avoid any premature exposure of the membrane, which could compromise the resorption kinetics and the success of the regeneration. The manufacturer Hyundai Bioland emphasizes that careful reading of the instructions is indispensable to master the methods of use and ensure patient safety throughout the healing phase.

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

The T-GEN resorbable collagen membrane is manufactured by the specialized company Hyundai Bioland Co., Ltd. This medical device complies with current regulations, being listed as Class III, which corresponds to the highest level of requirement for implantable medical devices. This classification guarantees that the Hyundai Bioland product has undergone rigorous evaluations regarding its safety and clinical performance within the framework of tissue regeneration and implantology. Regulatory compliance marking assures dental surgeons and implantologists of the use of material meeting the quality standards required for complex oral surgery interventions.

State of the art

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