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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Vidar Systems with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 2013: TELERADPRO EDGE; TELERADPRO EDGE HD-CCD.
| Date | Record | Source |
|---|---|---|
| Jun 7, 2013 | TELERADPRO EDGE; TELERADPRO EDGE HD-CCDK130636 · LMA | 510(k) clearances |
| Apr 29, 2013 | DIAGNOSTICPRO EDGEK130406 · LMA | 510(k) clearances |
| Oct 7, 2010 | TELERADPROK102476 · LMA | 510(k) clearances |
| Jan 7, 2010 | VIDAR DENTAL FILM DIGITIZERK093809 · LMA | 510(k) clearances |
| May 30, 2007 | VIDAR VISION 3000 AND 4000 X-RAY SYSTEMSK071193 · MQB | 510(k) clearances |
| Mar 16, 2007 | VIDAR VISION 2000K070563 · MQB | 510(k) clearances |
| Mar 4, 2003 | VIDAR BONE TRACK SYSTEM SOFTWAREK024171 · JAK | 510(k) clearances |
| Oct 1, 2001 | EXPRESSSUITEK011049 · LMA | 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
