3D LifeViz® Mini

About the Camera

3D Clinical imaging in a compact stereovision camera

LifeViz MINI 

Precise, Validated & Compact 3d Technology

The 3D LifeViz® Mini is compact, portable and wireless to enable the Investigators to move freely and save space in their research facility.

The results are superior quality 3D images which generate precise and accurate quantitative measurements ideally suited for clinical trials.


Image quality and reproducibility

The dual beam pointers and ‘LiveView’ function allow correct image orientation and acquisition at a fixed distance from the subject without the need for a repositioning device.

Simple and objective, the system will ensure greater image reproducibility and standardization without any skin contact.



About the Software

Accurate & precise 3d analysis

The 3D LifeViz® Mini system has been validated for a variety of skin measures including:

Volume Perimeter Width Average depth
Surface Length Distance Height, etc.


3D imaging and analysis enables accurate and reliable measurements to track treatment efficacy and conduct clinical research with confidence.


Ideal For?

A wide range of clinical applications

The 3D LifeViz® Mini system allows you to document and analyze data regarding the efficacy and safety of new products.

The 3D LifeViz® Mini can be an ideal tool to help generate publications in a multitude of domains and effectively support and accelerate the clinical research process in the following clinical areas:

  • Wound care (diabetic foot ulcers, venous leg ulcers, burns, etc.)
  • Infectious diseases (ABSSSi, abscesses, etc.)
  • Dermatology (psoriasis, actinic keratosis, vitiligo, rosacea, etc.)
  • Aesthetic (cellulitis, laser, dermal fillers, body contouring, botulinium toxin, submental fat, etc.)

Centralization & integration in clinical trial services

The 3D LifeViz® system is supported by a comprehensive set of clinical trial services facilitating all phases of the clinical development process.

Images are centralized for quality checks, objective analysis, expert assessments and archiving in conformance with FDA 21CFR Part 11 and EU guidance.