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 AmplifonLabelled by claude-sonnet-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 13, 2026, FDA's public records list Dahlberg Electronics, Inc. with 31 510(k) clearances. The most recent is a 510(k) clearance dated Jan 22, 1990: DAHLBERG MODEL LP BEHIND-THE-EAR HEARING AID.
| Date | Record | Source |
|---|---|---|
| Jan 22, 1990 | DAHLBERG MODEL LP BEHIND-THE-EAR HEARING AIDK896159 · ESD | 510(k) clearances |
| Jan 22, 1990 | DAHLBERG MODEL LH BEHIND-THE-EAR HEARING AIDK896157 · ESD | 510(k) clearances |
| Jan 22, 1990 | DAHLBERG MODEL LA BEHIND-THE-EAR HEARING AIDK896158 · ESD | 510(k) clearances |
| Jun 7, 1988 | DAHLBERG MODEL GP BODY AIDK881417 · ESD | 510(k) clearances |
| Jun 1, 1988 | DAHLBERG MODEL XJ 8080 BODY-WORN HEARING AIDK881612 · ESD | 510(k) clearances |
| Feb 22, 1988 | AUDIOTONE MODEL A2000 BEHIND-THE-EAR HEARING AIDK874831 · ESD | 510(k) clearances |
| Feb 17, 1988 | MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AIDK874830 · ESD | 510(k) clearances |
| Sep 16, 1987 | DAHLBERG MODEL GH BODY AIDK873169 · 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
