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 Western Advanced Technology with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 12, 1983: SYSTEM 80 FACEPLATE-IN-THE-EAR #F1.
| Jul 12, 1983 | SYSTEM 80 FACEPLATE-IN-THE-EAR #F1K822411 · EIB | 510(k) clearances |
| Jan 19, 1982 | AUDITORY STIMULATORK813557 · ETS | 510(k) clearances |
| Aug 20, 1981 | TENS DEVICEK812138 · GZJ | 510(k) clearances |
| Jul 15, 1981 | AUDITORY LOCALIZERK811772 · ETS | 510(k) clearances |
| Jul 15, 1981 | OCTOTOXIC SCREENERK811790 · ETS | 510(k) clearances |
| Oct 10, 1980 | E1 SERIES HEARING AIDK802324 · 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
