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Addressing Clinical Challenges in GBR with Resorbable Collagen Membranes

Reliable Barrier Function for Guided Bone Regeneration

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Released By Maxigen Biotech Inc.

Guided bone regeneration (GBR) relies heavily on collagen membranes for their outstanding biocompatibility and ability to support tissue healing. However, selecting the ideal collagen membrane remains a clinical challenge. The membrane must possess sufficient mechanical strength to endure surgical manipulation without tearing, while remaining flexible enough to closely adapt to irregular bone defects.

Equally important is the membrane’s degradation profile. It should maintain a stable barrier during critical bone regeneration phases to prevent soft tissue invasion, which can impair new bone formation. At the same time, it must resorb in harmony with natural healing to avoid prolonged foreign body presence and eliminate the need for secondary surgeries. Clinicians often face problems such as premature membrane breakdown, inadequate space maintenance, or delayed resorption, all of which threaten clinical success. Complex cases, such as those with thin gingival biotypes, large defects, or immediate implant placements, require membranes that combine durability, adaptability, and predictable resorption.

Reflecting a broader trend in dental biomaterials, the demand for optimized collagen membranes is rising. According to the 2024 Coherent Market Insights report, the global market for dental membranes and bone graft substitutes is projected to exceed USD 1.4 billion by 2031. This growth is driven by increased use of absorbable membranes that enhance patient comfort by removing the need for secondary surgeries and improving surgical predictability.

In this evolving landscape, collagen membranes that effectively balance mechanical performance, biological integration, and controlled biodegradation are becoming indispensable for modern implant dentistry.

Ideal Collagen Membrane for GBR with High Strength and Biocompatibility

FormaAid® Collagen Membrane is made from highly purified Type I bovine tendon collagen using physical crosslinking instead of chemical methods. This process preserves the natural collagen structure while delivering high tensile strength and excellent durability. Designed for use in both dry and wet conditions, it forms an effective natural barrier that supports optimal guided bone regeneration.

Its unique double-layer technology further enhances clinical performance by improving space maintenance and barrier function. The membrane offers superior biocompatibility and excellent suturability, allowing for easier and more precise surgical handling. For clinical case studies and detailed application guidance, please contact us.

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