Xoft, Inc.
Xoft, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 16, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K090914 | AXXENT BALLOON APPLICATOR, MODEL AB2034, AB2045, AB2056, AB2057E, AB2067E | July 16, 2009 |
| K090417 | AXXENT FLEXISHIELD MINI | June 23, 2009 |
| K083734 | AXXENT SURFACE APPLICATOR, MODEL 710257 | February 11, 2009 |
| K072616 | AXXENT VAGINAL APPLICATOR | May 9, 2008 |
| K072683 | AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM | February 29, 2008 |
| K050843 | AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM | December 22, 2005 |