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 Bosch Hearing Instruments, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1985: EKG 501 A.
| Dec 30, 1985 | EKG 501 AK840569 · DPS | 510(k) clearances |
| Dec 30, 1985 | EKG 503AK840571 · DPS | 510(k) clearances |
| Nov 14, 1985 | EBM-500K840574 · DXN | 510(k) clearances |
| Sep 30, 1982 | BOSCH STAR 66F-SP HEARING AIDK822579 · ESD | 510(k) clearances |
| Jan 22, 1982 | BOSCH TOP STAR IIIK820041 · ESD | 510(k) clearances |
| Mar 31, 1981 | BOSCH STAR 66F SUPER EARLEVEL AIDK810347 · ESD | 510(k) clearances |
| Jun 4, 1980 | OMNITON MT80-A BODY HEARING AIDK800779 · 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
