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 14, 2026, FDA's public records list Iomed, Inc. with 17 510(k) clearances and 1 drug application. The most recent is a 510(k) clearance dated Feb 28, 2007: CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICE.
| Feb 28, 2007 | CHAMPION IONTOPHORETIC DRUG DELIVERY DEVICEK063465 · EGJ | 510(k) clearances |
| Mar 31, 2006 | MW-1000 IONTOPHORETIC DRUG DELIVERY ELECTRODEK060236 · EGJ | 510(k) clearances |
| Dec 22, 2003 | RH-950K033192 · KTB | 510(k) clearances |
| Jul 10, 2003 | RH-900K031115 · KTB | 510(k) clearances |
| Oct 18, 2000 | TRANSQ3K001522 · KTB | 510(k) clearances |
| Aug 1, 2000 | PHORESOR MODEL PM2000K001410 · KTB | 510(k) clearances |
| Mar 2, 1999 | PHORESOR II,MODEL PM900K982668 · EGJ | 510(k) clearances |
| Mar 27, 1998 | PHORESOR II, MODEL PM900K974855 · KTB | 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
