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. Author manuscript; available in PMC: 2015 Aug 1.
Published in final edited form as: Urol Oncol. 2013 Nov 13;32(6):903–911. doi: 10.1016/j.urolonc.2013.08.006

Table.

MR-US fusion devices approved by the US Food and Drug Administration. Reprinted with permission from Marks et al. [50]

Manufacturer/trade
name
US image acquisition Biopsy route Tracking mechanism Year of FDA
approval
Comments
Philips/UroNav Manual US sweep from base
  to apex
Transrectal External magnetic field
  generator
2005 Prospective targeting,
  integrated with existing
  ultrasound device, freehand
  manipulation
Eigen/Artemis Manual rotation along fixed
  axis
Transrectal Mechanical arm with
encoders
2008 Prospective targeting,
  stabilized TRUS probe
Koelis/Urostation Automatic US probe rotation,
  3 different volumes
  elastically registered
Transrectal Real-time TRUS-TRUS
  registration
2010 Retrospective targeting, real
  time elastic registration
Hitachi/HI-RVS
  (real-time virtual
  sonography)
Real-time biplanar TRUS Transrectal or
  transperineal
External magnetic field
  generator
2010 Prospective targeting,
  integrated with existing
  ultrasound device
BioJet/Jetsoft/
  GeoScan
Manual US sweep in sagittal Transrectal or
  transperineal
Mechanical arm with
  encoders; uses stepper
2012 Prospective targeting, rigid
  registration