Resorbable collagen membrane 30X40 mm T-GEN - Hyundai Bioland - Delynov

What is the Hyundai Bioland T-GEN 30X40 mm membrane?

The Hyundai Bioland T-GEN membrane is a medical device designed for guided bone regeneration (GBR). Presented here in a 30X40 mm format, this dental collagen membrane is specifically developed to serve as a biological barrier. Its structure is optimized to maintain the space necessary for bone neoformation while preventing the invasion of epithelial and connective soft tissues within the graft site. Manufactured by Hyundai Bioland Co., Ltd, it fits into surgical protocols requiring high biocompatibility and ease of handling for the practitioner.

What are the clinical indications for this collagen membrane?

This resorbable implantology membrane is indicated for various oral and maxillofacial surgery interventions. It is primarily used for filling peri-implant bone defects, alveolar ridge preservation after extraction, or during sinus lifts. Its 30X40 mm dimension allows for covering significant surfaces, facilitating the stabilization of bone filling materials. Using this resorbable gbr membrane secures the healing process by creating a protected environment conducive to osteoconduction and osseointegration of implants.

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

The T-GEN membrane is distinguished by its mechanical properties and clinical handling. With dimensions of 30X40 mm, it offers a generous coverage surface for complex cases. As a dental collagen membrane, it possesses remarkable anatomical adaptation capacity once moistened, perfectly matching the contours of the surgical site. Its structure is designed to offer sufficient tear resistance during placement and fixation, while maintaining adequate porosity for the nutritional exchanges necessary for tissue regeneration without compromising its barrier function.

What are the contraindications for the use of this device?

Like any implantable device, the use of the Hyundai Bioland membrane is subject to rigorous clinical evaluation. General contraindications include uncontrolled systemic pathologies affecting bone healing or collagen metabolism. Although specific details are not provided here, practitioners must ensure the absence of known hypersensitivity to porcine or bovine-derived components generally used for these devices. It is imperative not to use the product in case of active infection at the operative site or insufficient vascularization of the surrounding tissues.

How does resorption occur and what are the precautions?

The T-GEN membrane is a resorbable gbr membrane, meaning it is naturally eliminated by the body, thus avoiding a second surgical intervention for its removal. The resorption process occurs progressively, with the duration depending on the patient's metabolism and the enzymatic environment of the site. To guarantee the effectiveness of the barrier, the practitioner must ensure hermetic closure of the flaps to avoid any premature exposure of the membrane to the oral environment, which could accelerate its degradation and compromise the underlying bone regeneration.

Who is the manufacturer and what standards are respected?

The official manufacturer of this device is Hyundai Bioland Co., Ltd, a recognized player in the field of biomaterials. The production of the T-GEN membrane follows rigorous manufacturing protocols to ensure the safety and quality of the final product. For any information regarding specific certifications, such as CE marking or the exact regulatory class, it is recommended to systematically refer to the instructions for use and labeling provided by Hyundai Bioland. Compliance with aseptic protocols and manufacturer recommendations is essential to ensure the conformity of clinical use.

State of the art

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