Products›Socko Medical Product›Moldable Collagen Bone Graft
Bone Graft & Biomaterials

Moldable Collagen Bone Graft

Moldable collagen-based bone graft options from the Graftend and Goalie product families.

Moldable Collagen Bone Graft
Product type
Bone Graft & Biomaterials
Application
Bone Graft & Biomaterials
Manufacturer / Brand
Socko Medical Co., Ltd.
Regulatory
Graftend TFDA No. 007887 / Goalie TFDA No. 008321
Product Overview

Moldable Collagen Bone Graft

This product family groups the moldable configurations of Socko Medical's collagen-based bone graft portfolio. The material can be shaped for placement into suitable bone defects or gaps according to each product's approved Instructions for Use.

Material / PlatformCollagen-based bone graft materials; approved product labeling should be consulted for model-specific composition and handling.
Design & Product Features

Moldable presentation

Graftend and Goalie product options

Sterile single-use configurations

Adaptable shaping for defect filling

Technical Information

Models & specifications

Configurations shown here are a website summary. Use the current approved product documentation for final model selection and procedural details.

Graftend Moldable: 2 mL

Goalie Moldable: 1 mL

Model-specific preparation and handling requirements follow the approved IFU

Sterility / Processing

Sterile, single use; refer to the applicable approved IFU and labeling for each product.

Clinical Profile

Indications overview

The points below summarize the product family. Final patient selection and clinical use must follow the applicable approved labeling and Instructions for Use.

01

Filling suitable bone defects or gaps as described in the approved IFU

02

Moldable handling for defect adaptation where clinically appropriate

03

Use as a graft material rather than a structural load-bearing implant

Moldable Collagen Bone Graft product visual
Product Visualization

Moldable Collagen Bone Graft

Product imagery is provided for portfolio identification. Model-specific components, dimensions and technique should be confirmed against current approved documentation.

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