In pre-clinical open (onlay) porcine studies conducted by XyberCyl, XyberCyl and a leading surgical mesh product (Product “P”) were implanted. Non-implanted control areas were designated in each test subject. The results were quite compelling: XyberCyl was superior to Product “P” in every parameter.
In pre-clinical laparoscopic porcine studies conducted for XyberCyl by Dr. Salvador Morales-Conde in Spain, XyberCyl and a leading surgical mesh product (Product “V”) were implanted. The results were quite compelling: XyberCyl was superior or equivalent to Product “V” when measuring key parameters.
The issues with surgical mesh (e.g. shrinkage, chronic pain, chronic infection, failure, etc.) are well-known, and have been well-documented and well-litigated.
New product releases by surgical mesh companies have many times been innovative – addressing one specific issue, yet ignoring other serious issues. For example, Product “V” acquired an innovative coating technology that significantly reduces the risk of adhesions – yet this mesh is still recognized as a foreign body, often shrinks and even folds. Product “U” is innovative in that it is large-pore – allowing for better integration into the surrounding tissue – yet its knitted construct generates a foreign-body reaction with all of its related issues.
XyberCyl, on the other hand, is both innovative and inclusive – an innovative construct that is invisible to the human body and inclusively addresses all issues typically experienced with other surgical meshes.
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