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Xoft, Inc.

FDA Regulatory Profile

Xoft, Inc. has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 16, 2009

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances6Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K090914AXXENT BALLOON APPLICATOR, MODEL AB2034, AB2045, AB2056, AB2057E, AB2067EJul 16, 2009
K090417AXXENT FLEXISHIELD MINIJun 23, 2009
K083734AXXENT SURFACE APPLICATOR, MODEL 710257Feb 11, 2009
K072616AXXENT VAGINAL APPLICATORMay 9, 2008
K072683AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMFeb 29, 2008
K050843AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMDec 22, 2005

FDA data resources