
Medical Device Manufacturer

Cervical and Lumbar Interbody Fusion Device Developer

NanovisNanovis (Ti Surface) is the first to receive FDA approval for using nanocoating technology on PEEK implant surface modification, and also the world's first to receive FDA approval for nano-modification technology on pedicle screw surfaces.

According toNanovisIntroductionNanovis (Ti Surface)With controlled nanostructured surfaces composed of nanotube arrays, the average pore size is between 60-80 nanometers. Compared to other surfaces commonly used in orthopedics, these nanotube arrays have been shown to increase and accelerate the production of calcified extracellular matrix on human osteoblasts and human mesenchymal stem cells in vitro within 21 days.

Ti SurfaceThe technology not only accelerates bone cell growth and the fusion of human tissue with implants, but also has significant economic cost value. According to them,Study: Its cost may be 1/3 to 1/2 of other surface modification technologies (e.g., hydroxyapatite (HAP)), without the various clinical issues associated with hydroxyapatite.
NanovisBy virtue ofTi SurfaceTechnology, by GlobRecognized by al Health and Pharma as the best nanotechnology-driven implant company, and by Med Tech Outlook as one of the top ten orthopedic solution providers.
NanovisIn addition to surface modification technologies, the following spinal implants are also available:



Nanovis
Nanovis is aA technology-driven innovative company dedicated to discovering unmet clinical needs, developing innovative and enabling solutions, and validating new technologies for clinical and market acceptance.Developed a market-leading nanotube surface technology, which has been proven to improve the osseointegration of titanium implants.

