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

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

The 30X40 mm T-GEN resorbable collagen membrane, distributed by Delynov, is a medical device designed specifically for Guided Bone Regeneration (GBR) procedures. Manufactured by Hyundai Bioland Co., Ltd, this membrane is composed of collagen, a material recognized for its biocompatibility properties in oral surgery. Its structure is optimized to serve as a protective barrier during bone grafts, thus promoting tissue healing while preventing soft tissue invasion into the bone defect. Its 30X40 mm dimensions allow for the coverage of significant surgical surfaces, offering flexibility of use to implantologists and dental surgeons.

What are the clinical indications for the T-GEN membrane?

In dental and implant surgery, the Hyundai Bioland collagen membrane is primarily indicated for Guided Bone Regeneration (GBR) and Guided Tissue Regeneration (GTR) interventions. It is used to stabilize the bone filling material and protect the surgical site during the neo-vascularization phase. Its use is common during ridge augmentations, the treatment of periodontal defects, or alveolar preservation after extraction. Thanks to its resorbable composition, it eliminates the need for a second surgical intervention for its removal, thus simplifying the clinical protocol for both the practitioner and the patient.

What are the technical characteristics of the 30X40 mm membrane?

The T-GEN membrane from Hyundai Bioland features technical characteristics adapted to the requirements of oral surgery. With a generous 30X40 mm format, it offers a wide coverage area for extensive bone defects. Its collagen structure gives it excellent clinical handling, allowing for precise adaptation to the anatomical contours of the recipient site. This device is designed to maintain its structural integrity during the critical period of regeneration, while being completely resorbable by the body. Its design by Hyundai Bioland Co., Ltd ensures manufacturing quality that meets the standards of medical devices intended for implantology.

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

The use of the T-GEN resorbable collagen membrane from Hyundai Bioland is contraindicated in patients with a known hypersensitivity or allergy to collagen or to porcine/bovine components depending on the origin of the material. It must not be applied to sites with active infection or uncontrolled inflammation. As with any GBR device, insufficient vascularization of the site or inadequate tissue coverage can compromise the success of the regeneration. It is imperative for the practitioner to consult the instructions for use provided by the manufacturer Hyundai Bioland Co., Ltd before any intervention to verify all precautions for use.

How does resorption occur and what precautions should be taken?

The T-GEN membrane is a resorbable device, meaning it is progressively degraded by the natural enzymatic processes of the human body. This mechanism avoids a subsequent surgical removal procedure. The duration of the barrier function maintenance is optimized to allow for the formation of new healthy bone. To guarantee an optimal result, the practitioner must ensure hermetic closure of the soft tissues without tension to avoid any early exposure of the membrane, which could accelerate its resorption and compromise the underlying regeneration. Handling must be done with sterile instruments according to the rigorous asepsis protocols of implant surgery.

Who is the manufacturer and what are the quality guarantees?

The official manufacturer of this device is Hyundai Bioland Co., Ltd, a company specializing in biotechnology and medical devices. The brand Hyundai Bioland is internationally recognized for its expertise in the development of tissue regeneration solutions. Although detailed regulatory specifications (class, specific CE marking) must be verified directly on the labeling and accompanying instructions of the product delivered by Delynov, the manufacturing process follows strict industrial standards. Each 30X40 mm membrane is packaged to guarantee its sterility until its use in the operating room, thus ensuring maximum safety for oral surgery interventions.

State of the art

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