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 13, 2026, FDA's public records list Aurora Imaging Technology with 7 510(k) clearances. The most recent is a 510(k) clearance dated Sep 16, 2008: MODIFICATION TO AURORA MRI SYSTEM.
| Date | Record | Source |
|---|---|---|
| Sep 16, 2008 | MODIFICATION TO AURORA MRI SYSTEMK073425 · LNH | 510(k) clearances |
| Nov 8, 2005 | MODIFICATION TO: AURORAK052698 · LNH | 510(k) clearances |
| Sep 24, 2003 | MODIFICATION TO: AURORAK032678 · LNH | 510(k) clearances |
| Jul 30, 2003 | AURORAK032082 · LNH | 510(k) clearances |
| Jan 29, 2003 | AURORA MR-GUIDED INTERVENTIONAL SYSTEMK023686 · LNH | 510(k) clearances |
| Sep 19, 2001 | AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICEK012154 · LNH | 510(k) clearances |
| Feb 21, 2001 | AURORAK003651 · LNH | 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
