Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Xoft, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jul 20, 2011: AXXENT RADIATION SHIELD - RIGID.
| Date | Record | Source |
|---|---|---|
| Jul 20, 2011 | AXXENT RADIATION SHIELD - RIGIDK111299 · JAD | 510(k) clearances |
| Jul 16, 2009 | AXXENT BALLOON APPLICATOR, MODEL AB2034, AB2045, AB2056, AB2057E, AB2067EK090914 · JAD | 510(k) clearances |
| Jun 23, 2009 | AXXENT FLEXISHIELD MINIK090417 · IXI | 510(k) clearances |
| Feb 11, 2009 | AXXENT SURFACE APPLICATOR, MODEL 710257K083734 · JAD | 510(k) clearances |
| May 9, 2008 | AXXENT VAGINAL APPLICATORK072616 · JAD | 510(k) clearances |
| Feb 29, 2008 | AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMK072683 · JAD | 510(k) clearances |
| Dec 22, 2005 | AXXENT ELECTRONIC BRACHYTHERAPY SYSTEMK050843 · JAD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
