Stereotaxis Inc

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
27
Inspections
4
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0430-2021Class IINiobe ES System, Models 001-006000-1 and 001-006100-1September 21, 2020

Recent 510(k) Clearances

K-NumberDeviceDate
K251792Stereotaxis GenesisX RMN with Navigant ™ Workstation (NWS)November 6, 2025
K250590MAGiC Sweep™ EP Mapping CatheterJuly 23, 2025
K193147Stereotaxis Genesis RMN with Navigant Workstation (NWS) and Cardiodrive SystemMarch 5, 2020
K192775Niobe® Magnetic Navigation System (MNS) with Navigant Workstation (NWS) and CardiodriOctober 30, 2019
K183027Steerable catheter control systemSeptember 6, 2019
K150312Vdrive system, Vdrive Duo, Vdrive with V-SonoJune 17, 2015
K141530VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CASDecember 18, 2014
K140804VDRIVE WITH V-LOOP/ VDRIVE DUOSeptember 3, 2014
K133396VDRIVE WITH V-SONOFebruary 6, 2014
K122659VDRIVE W/V-SONOJuly 26, 2013
K093092ODYSSEY WORKSTATIONJanuary 21, 2010
K080637POWERASSET RADIOFREQUENCY GUIDWIRE, MODEL VARIOUSAugust 12, 2008
K072371ODYSSEY WORKSTATIONNovember 14, 2007
K071029CARDIODRIVE CATHETER ADVANCEMENT SYSTEM (CAS)August 24, 2007
K060967NIOBE MAGNETIC NAVIGATION SYSTEM W/NAVIGANT WORKSTATIONOctober 19, 2006
K042850CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)August 9, 2006
K051760NAVIGANT WORKSTATION WITH NIOBE MAGNETIC NAVIGATION SYSTEM, MODEL NWS05May 5, 2006
K051373CRONUS GUIDEWIRE, MODEL 001-001470-1December 9, 2005
K051374CARDIODRIVE CATHETER ADVANCEMENT SYSTEMJune 23, 2005
K043457MODIFICATION TO ENDOVASCULAR GUIDE WIREFebruary 28, 2005