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 GN Store NordLabelled 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 ReSound with 41 510(k) clearances. The most recent is a 510(k) clearance dated Mar 19, 1999: DIGITAL LGOB PROCEDURE USING RESOUND, DIGITAL 5000 SERIES HEARING AIDS.
| Mar 19, 1999 | DIGITAL LGOB PROCEDURE USING RESOUND, DIGITAL 5000 SERIES HEARING AIDSK984547 · EWO | 510(k) clearances |
| Dec 12, 1997 | RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)K974257 · ESD | 510(k) clearances |
| Dec 12, 1997 | RESOUND STEALTH CICK974081 · ESD | 510(k) clearances |
| Jul 3, 1997 | RESOUND ED4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTIONK971605 · ESD | 510(k) clearances |
| Mar 31, 1997 | AUDALLION II HEARING SYSTEMK970215 · ESD | 510(k) clearances |
| Nov 27, 1996 | RESOUND BT4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTIONK964557 · ESD | 510(k) clearances |
| Nov 4, 1996 | RESOUND CC4 PERSONAL HEARING SYSTEMK964115 · ESD | 510(k) clearances |
| Apr 10, 1996 | RESOUND PERSONAL HEARING SYSTEMS EDR ENCORE SERIES MODELS EDR-E, EDR-ES, EDR-EV, & EDR-P1K960680 · 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
