Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FinlandLabelled 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 Soredex Palodex Group Oy with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 30, 2011: SCANORA 3D.
| Jun 30, 2011 | SCANORA 3DK110839 · OAS | 510(k) clearances |
| Dec 19, 2007 | SCANORA 3DK073350 · MUH | 510(k) clearances |
| Mar 27, 2007 | DIGORA PCT/DIGIPODK070304 · MUH | 510(k) clearances |
| Dec 26, 2006 | CRANEX NOVUSK063459 · MUH | 510(k) clearances |
| Dec 17, 2004 | CRANEX DK043307 · EHD | 510(k) clearances |
| Jul 13, 2004 | CRANEX BASEX D OR CRANEX EXCEL DK040382 · EHD | 510(k) clearances |
| Jun 15, 2004 | DIGORA OPTIME (OR DIGORA ONTIME)K041050 · MUH | 510(k) clearances |
| Apr 29, 2004 | MINRAYK033755 · EHD | 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
