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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Magnatone Hearing Aid Corp. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 22, 2010: EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICE.
| Dec 22, 2010 | EVOK 900 SERIES HEARING AID/TINNITUS MASKER OPTION DEVICEK093715 · KLW | 510(k) clearances |
| Nov 19, 1997 | FUTURA 67M, 68M, MEGAPOWERMP97, INTEGRA 70,71,72,73, SUPRA 51,52, SUPRA 56,57,58,59, SUPREMA 45, 46, 47,48K973861 · ESD | 510(k) clearances |
| Nov 4, 1997 | MAGNATONE / STERLING/ ST; MAGNATONE/DB; MAGNATONE/ LIBERTY/ LB; MAGNATONE/ PEARL/PH C.I.C., S.P.I., ONE TOUCH, DESIGNERK973665 · ESD | 510(k) clearances |
| Nov 16, 1994 | MAGNATONE MODEL M PREWIRED FACEPLATE HEARING AIDK944241 · ESD | 510(k) clearances |
| Jul 9, 1991 | NHS 2044P BODY AID, HEARING AIDK911183 · ESD | 510(k) clearances |
| May 9, 1991 | NNHS 2050 SERIES (2055W-2054PP) HEARING AIDSK911182 · ESD | 510(k) clearances |
| May 9, 1991 | NHS 2009SP HEARING AIDK911174 · ESD | 510(k) clearances |
| May 19, 1989 | INTERTON BTE HEAR AID, SUPRA, SUPREMA, MINETTAK890525 · 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
