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 15, 2026, FDA's public records list Diomed, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 25, 2007: DIOMED DELTA 25.
| Jan 25, 2007 | DIOMED DELTA 25K063828 · GEX | 510(k) clearances |
| Aug 18, 2005 | DIOMED DELTA 15, MODEL DELTA 15; DIOMED DELTA 30, MODEL DELTA 30K051996 · GEX | 510(k) clearances |
| Dec 1, 2004 | EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERSK041957 · GEX | 510(k) clearances |
| Dec 2, 2002 | EVLT KIT AND D15PLUS AND D30PLUS DIODEK023543 · GEX | 510(k) clearances |
| Jan 22, 2002 | DIOMED 15 DIODE LASERK012398 · GEX | 510(k) clearances |
| Nov 16, 2001 | DIOMED 15 PLUS AND DIOMED 30PLUS LASERSK013499 · GEX | 510(k) clearances |
| May 1, 2000 | A100 AESTHETIC DIODE LASERK000982 · GEX | 510(k) clearances |
| Feb 26, 1999 | DIOSCANK990014 · GEX | 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
