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 14, 2026, FDA's public records list Trutone with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 10, 1998: SIBELMED AC50D.
| Mar 10, 1998 | SIBELMED AC50DK973377 · EWO | 510(k) clearances |
| Jul 31, 1997 | AUDIFON H24 AGC/AUDIFON H25 AGC/AUDIFON H30 AGCK972550 · ESD | 510(k) clearances |
| Jul 30, 1997 | AUDIFON H20 PC/AUDIFON H32 PPK972552 · ESD | 510(k) clearances |
| Jul 23, 1997 | JAZZ PP AGC-O, JAZZ PPK972542 · ESD | 510(k) clearances |
| Jul 23, 1997 | TWIST PPAGC-1, TWIST PPK972543 · ESD | 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
