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 its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Micro-Ear Technology with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 1, 2004: REFUGE SOUND GENERATOR.
| Jul 1, 2004 | REFUGE SOUND GENERATORK041302 · KLW | 510(k) clearances |
| Jul 23, 1997 | MERIDIAN DSPK972431 · ESD | 510(k) clearances |
| Jun 6, 1997 | POWER D, TRU 5, PERSONA, PERSONA CHOICE, MERIDIANK970880 · ESD | 510(k) clearances |
| Feb 11, 1997 | SUPER K-AMP, EZ-COMPRESSION, TRIM-PRO, HF-PRO, ENVIRO-PRO, COMPRESSION-PRO, COMPRESSION 3000, HF 3000, OCTIVA, REFLEX HFK964657 · ESD | 510(k) clearances |
| Dec 27, 1993 | MICRO-TECH TRU CANALK934149 · 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
