Sonova AG
Active in EUDAMEDSwitzerlandfrom SRN EUDAMED FDA SRN CH-MF-000015958 FEI 3005085999
- Devices
- 7,068
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 2 in force. 1 certificate has expired.
Market reach
- European Union
- EUDAMED actor, 2 certificates
- United States
- FDA FEI
- Authorised rep.
- Sonova Deutschland GmbHDE
What Sonova AG makes
Sonova AG manufactures various types of hearing aids including air-conduction hearing aids in different styles (behind-the-ear, receiver-in-canal, in-the-ear, and canal), as well as audiometric/hearing device software, hearing aid enhanced audio devices for teaching environments, noninvasive device battery chargers, and audiometric/hearing aid testers.
The company's portfolio includes devices classified under Class I, Class II, and Class IIa, and is listed in the eudamed and fda_udi registries. Sonova AG is based in Switzerland (CH).
Catalogue
Search and filter all 7,068 devicesShowing 1-50 of 7,068
Company details
- EUDAMED SRN
- CH-MF-000015958
- FDA FEI number
- 3005085999
- DUNS number
- 480662550
- EUDAMED status
- Active
- EUDAMED registered name
- Sonova AG
- Registered address
- 8712, Staefa, Switzerland
- [email protected]
- Phone
- +41589280101
- PRRC contact
- Blathnaid Feldman
EUDAMED certificates
2 certificates1 valid, 1 expiredMDR 2next expiry 8 Nov 2031
GMED SAS 0459 2 certificates
- 38657 Active
Quality management system EU MDR
- Issued
- 5 Oct 2026
- Expires
- 8 Nov 2031
- Valid from
- 9 Nov 2026
- 38657 Expired
Quality management system EU MDR
- Issued
- 9 Jul 2026
- Expires
- 8 Nov 2026
- Reason
- Add device or group
Frequently asked questions
How many devices does Sonova AG have in the registry?
The registry currently lists 7068 devices for Sonova AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sonova AG's devices?
Among its 50 most recently registered devices, Sonova AG has devices listed in EUDAMED (50 devices).
What risk classes do Sonova AG's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Sonova AG's devices are Class I and Class IIa. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Sonova AG?
EUDAMED lists 2 certificates for Sonova AG (quality management system) under MDR. The most recent was issued on 5 Oct 2026.
What are the newest devices from Sonova AG in the registry?
The most recently registered devices listed for Sonova AG include AudioNova B1-PR (espresso), otofarma ODI UP (sand), Insera B7-312 (L DV3U PM MM WH P) and excellence 4 312 Select (platinum).