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., part of Miracle-EarLabelled 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 15, 2026, FDA's public records list Miracle-Ear/Dahlberg, Inc. with 23 510(k) clearances. The most recent is a 510(k) clearance dated Aug 17, 1994: MIRACLE-EAR MODEL PGF + REMOTE.
| Aug 17, 1994 | MIRACLE-EAR MODEL PGF + REMOTEK942893 · ESD | 510(k) clearances |
| Aug 17, 1994 | MIRACLE EAR MODEL PGMK942895 · ESD | 510(k) clearances |
| Aug 17, 1994 | MIRACLE-EAR MODEL PGCK942894 · ESD | 510(k) clearances |
| Jul 25, 1994 | MIRACLE-EAR EAR IMPRESSION MATERIALK941859 · ESD | 510(k) clearances |
| Jun 23, 1986 | MODEL ED BEHIND-THE-EAR HEARING AIDK862100 · ESD | 510(k) clearances |
| Jun 23, 1986 | MODEL KM IN-THE-CANAL HEARING AIDK862102 · ESD | 510(k) clearances |
| Jun 23, 1986 | MODEL UC IN-THE-CANAL HEARING AIDK862103 · ESD | 510(k) clearances |
| Jun 23, 1986 | MODEL UC SPECTRUM IN-THE-CANAL HEARING AIDK862104 · 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
