Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list I.Z.I. Corp. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Aug 13, 2002: SPHERZ.
| Aug 13, 2002 | SPHERZK022074 · HAW | 510(k) clearances |
| Mar 4, 2002 | MRI LINE MARKERK014022 · IYE | 510(k) clearances |
| Jan 18, 2001 | MRI LINE MARKERK003736 · JAK | 510(k) clearances |
| Feb 4, 2000 | MR ENHANCERK994117 · LNH | 510(k) clearances |
| Feb 2, 2000 | SUPER TISSUEK993742 · IYE | 510(k) clearances |
| Nov 19, 1993 | CT/MRI TOPOGRAPHIC MARKERK930752 · JAC | 510(k) clearances |
| Oct 16, 1992 | E.Z. PORT(TM) RADIATION THERAPY SKIN MARKERSK922287 · KPQ | 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
