The Four Pillars Of
Nanotechnology Healing

Heart icon Healing Benefits

Improves Inflammatory
Response

Reduces Bacterial
Colonization

Increases
Vascularization

Accelerates
Osseointegration

Nanotechnology is an engineered solution that addresses several overlapping issues.

These include bacterial colonization of the implant, inflammation around the implant, vascularization after implantation, and osseointegration. Solutions optimized for one of these problems may not solve others. We focused on innovating nanotechnology to address all four issues in a single approach.

Nanovis has successfully engineered our nanoVIS Ti™ Surface Technology to optimize implant integration from implantation to the end goal of osseointegration. 

  • Nanovis' nanotechnology increases protein attachment for a lower immune response. It also decreases inflammatory cell attachment and activation while encouraging pro-healing macrophages.
  • Our surface technology reduces bacterial colonization and biofilm formation and spread.
  • Our nanotubes speed up growth on the implant, supporting new bone growth and accelerates healing.
  • Osseointegration is the marker of successful implantation. The sooner bone firmly attaches to the implant, the better the outcome.

Our Solution

Technology
Description
nanoVIS Ti™ Surface Technology
An engineered, permanent nanotube surface technology applicable to any CP Titanium or Titanium Alloy Implant

Intellectual Property Protection

Nanovis® maintains a robust intellectual property portfolio consisting of several owned or licensed patents. All nanoVIS Ti™ Surface Technology components are protected by a series of patents. Additionally, the proprietary process used to produce our unique surface is safeguarded by multiple trade secrets.

Regulatory Strategy and Pathway

Nanovis® has achieved several significant regulatory milestones:

NanoVIS Ti™ Surface Technology is the only widely available platform nanotechnology to achieve FDA's nanotechnology designation.

We are the first company worldwide to obtain FDA clearance and nanotechnology designation for a pedicle screw system.

We are the second company worldwide to receive FDA clearance and nanotechnology designation for an interbody fusion cage.

The Master File for nanoVIS Ti™ Surface Technology has been referenced for multiple 510(k) clearances across two different product types in spine.

Screenshot of Nanovis Technology page

Manufacturing Operations

The application of nanoVIS Ti™ Surface Technology utilizes a validated manufacturing process that can fit within any supply chain. The flexibility of our proprietary process allows for the support of a wide range of quantities, both large and small, in an economical way.

Clinical and Commercial Advantages

To validate the nanoVIS Ti™ Surface Technology, Nanovis® has commercialized a portfolio of spinal products. Learn more at nanovisspine.com.

Nanovis' Nanotechnology

Clinical Advantages

  • FDA nanotechnology designation. First company in the world with designation on PEEK + Ti interbodies (CP Ti) and Open/MIS pedicle screws (ELI Ti).
  • Statistically significant and superior comparative surface data in the label – hMSC mineralization and osteoblast mineralization at 21 days, in vitro.
Nanovis' Nanotechnology

Commercial Benefits

  • On-label marketing for superior positioning and messaging.
  • Superior FDA label used to drive new surgeon conversions, hospital approvals, and technology price premiums.
  • Surface-on-a-surface story — add a nano surface to a macro-porous 3D-printed surface or a micron-roughened base.
  • Surgeon engagement at a scientific and innovation level, enabling studies, papers, podium presentations, etc.
Commercial products

Commercial Products

View Products
nanoVIS Ti™ Surface Technology

Discover the Data

Deep Dive
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technology.


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