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 Vicon Instrument Co. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 15, 1981: FINETONE MODEL VI HEARING AID.
| Jul 15, 1981 | FINETONE MODEL VI HEARING AIDK811751 · ESD | 510(k) clearances |
| Aug 3, 1979 | SCREENING AUDIOMETER, HIGH FREQUENCYK790878 · EWO | 510(k) clearances |
| Feb 16, 1979 | TINNITUS DEVICESK790064 · ETS | 510(k) clearances |
| Jan 3, 1978 | TINNITUS MASKERS, MODELS S564&S574K771769 · KLW | 510(k) clearances |
| Oct 4, 1977 | MODULAR HEARING DEVICE, MODEL S291K771762 · ESD | 510(k) clearances |
| Jun 28, 1977 | TINNITUS AID, MODEL S244K770938 · KLW | 510(k) clearances |
| Dec 16, 1976 | HEARING AIDS (MODEL E-552 S-712)K761216 · ESD | 510(k) clearances |
| Jul 21, 1976 | HEARING AID, S-522 FMK760215 · 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
