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Xoft, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K090914AXXENT BALLOON APPLICATOR, MODEL AB2034, AB2045, AB2056, AB2057E, AB2067EJuly 16, 2009
K090417AXXENT FLEXISHIELD MINIJune 23, 2009
K083734AXXENT SURFACE APPLICATOR, MODEL 710257February 11, 2009
K072616AXXENT VAGINAL APPLICATORMay 9, 2008
K072683AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMFebruary 29, 2008
K050843AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMDecember 22, 2005