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 Maico Hearing Instruments, Inc. with 58 510(k) clearances. The most recent is a 510(k) clearance dated Mar 7, 1996: AUDIOFLEX 120.
| Mar 7, 1996 | AUDIOFLEX 120K960031 · ESD | 510(k) clearances |
| Sep 28, 1995 | MAICO PRODIGY CIC SERIESK954054 · ESD | 510(k) clearances |
| Jul 24, 1995 | MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTIONK953161 · ETY | 510(k) clearances |
| Mar 21, 1995 | MAICO IN-THE-EAR MODEL RD-312 CICK950637 · ESD | 510(k) clearances |
| Jan 30, 1995 | MAICO IN-THE-EAR MODEL RD 201K946253 · ESD | 510(k) clearances |
| Aug 19, 1994 | KS 5 - CLINICAL AUDIOMETERK931322 · EWO | 510(k) clearances |
| Aug 23, 1993 | MAICO BTE MODEL RD-111 AND ITE MODEL RD-312 HEARING AIDK933291 · ESD | 510(k) clearances |
| Aug 5, 1993 | MAICO MA790 AUDIOMETERK930112 · EWO | 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
