Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled 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 Ab Ardent with 13 510(k) clearances. The most recent is a 510(k) clearance dated Nov 14, 2013: MERIDIAN.
| Nov 14, 2013 | MERIDIANK131753 · EBF | 510(k) clearances |
| Jul 20, 2004 | LATIT FLOWK040465 · EBF | 510(k) clearances |
| Nov 25, 2002 | MICROHYBRID 11K022971 · EBF | 510(k) clearances |
| Nov 22, 2002 | ADHESIVE 14K022973 · KLE | 510(k) clearances |
| Nov 22, 2002 | MICROHYBRID 12K022974 · EBF | 510(k) clearances |
| Nov 22, 2002 | ETCHING 15K022975 · EBF | 510(k) clearances |
| Nov 22, 2002 | MICROFILL 13K022972 · EBF | 510(k) clearances |
| May 7, 2002 | HIGH SILVER CONVENTIONALK020452 · EJJ | 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
