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 Marcon Hearing Instruments with 10 510(k) clearances. The most recent is a 510(k) clearance dated Dec 3, 1982: MODEL H 37E.
| Dec 3, 1982 | MODEL H 37EK823468 · ESD | 510(k) clearances |
| May 5, 1982 | MODEL IM9K821042 · ESD | 510(k) clearances |
| Oct 30, 1979 | MODEL H44-80 BEHIND THE EAR HEARINGK791745 · ESD | 510(k) clearances |
| Jul 17, 1979 | MODEL CE-DM-II HEARING INSTRUMENTK791126 · ESD | 510(k) clearances |
| Jul 5, 1979 | MODEL H63, BEHIND-THE-EARK790870 · ESD | 510(k) clearances |
| May 16, 1979 | MODEL H39C-BEHING-THE-EAR HEARING INSTRUK790779 · | 510(k) clearances |
| May 1, 1979 | BEHIND-THE-EAR, MODEL H37DK790727 · ESD | 510(k) clearances |
| May 1, 1979 | BEHIND-THE-EAR HEARING INSTRUMENT, H56K790700 · 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
