GoroRise Resorbable Collagen Membrane – Type I Collagen Barrier
GoroRise Resorbable Collagen Membrane: bovine pericardium-derived type I collagen; six rectangular sizes for oral regeneration. Use per professional evaluation/IFU.
Resorbable collagen membrane for guided bone regeneration workflows.
GoroRise Resorbable Collagen Membrane is derived from bovine pericardial tissue and is primarily composed of type I collagen. It retains the natural collagen fiber structure of the pericardial membrane and provides a resorbable barrier format for professional oral regenerative workflows.
Product overview
The supplied product brochure describes a thin, flexible and hydrophilic resorbable collagen membrane for barrier applications. Six rectangular sizes are available for different professional dental workflows.
Designed for barrier duration, flexibility and adaptation.
Long-lasting barrier
The membrane retains a dense collagen surface structure designed to limit epithelial-cell invasion and provide a sustained barrier effect.
Thin and flexible
The brochure describes mechanical strength and resistance to seam tearing, allowing use with sutures and membrane staples according to the applicable procedure.
Stabilized adhesion
The hydrophilic collagen membrane is designed to soften after infiltration, adapt to the treatment site and support stable placement.
Available membrane models and dimensions.
| Product number | Length | Width |
|---|---|---|
| OABM-1515 | 15 mm | 15 mm |
| OABM-2015 | 20 mm | 15 mm |
| OABM-2515 | 25 mm | 15 mm |
| OABM-3020 | 30 mm | 20 mm |
| OABM-4030 | 40 mm | 30 mm |
| OABM-6040 | 60 mm | 40 mm |
Barrier applications in oral regenerative workflows.
Applications listed in the supplied brochure
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Filling of extraction sockets
-
Expansion and reconstruction of the alveolar ridge
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Filling of periodontal bone defects
-
Alveolar ridge bone augmentation
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Maxillary sinus lift
For professional use. Product availability, labeling, specifications and approved indications may vary by market. Final selection and use must follow the applicable instructions for use, local regulatory requirements and professional clinical evaluation.
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