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Sign in to claim this brandSbo Hearing A/S
Denmark·DK-MF-000001270
Last updated May 26, 2026
What Sbo Hearing A/S makes
Sbo Hearing A/S manufactures air-conduction hearing aids in multiple form factors, including receiver-in-the-ear, behind-the-ear, in-the-ear, and canal designs. The company also produces wireless-fitting computer-aided software for hearing devices, remote controls for hearing aid/implant systems, and noninvasive battery chargers for hearing aids. These products are compatible with major brands such as Oticon, Philips, and EarQ.
The company’s portfolio includes devices classified as Class I and Class II under regulatory frameworks. Products are listed in the FDA’s Unique Device Identifier (UDI) database. Sbo Hearing A/S is based in Denmark.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Sbo Hearing A/S manufacture?
Sbo Hearing A/S specializes in air-conduction hearing aids across various form factors, including receiver-in-the-ear, behind-the-ear, in-the-ear, and canal designs. Their portfolio also includes wireless-fitting computer-aided software for hearing devices, remote controls for hearing aid/implant systems, and noninvasive battery chargers for hearing aids. These devices are designed to complement major brands like Oticon, Philips, and EarQ.
Where is Sbo Hearing A/S based?
Sbo Hearing A/S is headquartered in Denmark, as indicated by its regulatory and product documentation.
Which regulatory registries list Sbo Hearing A/S’s devices?
Sbo Hearing A/S’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which serves as a centralized registry for tracking medical devices authorized in the U.S. This inclusion helps ensure traceability and compliance with regulatory requirements.
How are Sbo Hearing A/S’s devices classified under regulatory frameworks?
Sbo Hearing A/S’s devices fall under Class I and Class II classifications, depending on their design, intended use, and associated risks. Class I devices generally pose minimal risk and may require fewer regulatory controls, while Class II devices involve moderate risk and may require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway and oversight required for each product.
Are Sbo Hearing A/S’s devices compatible with specific brands?
Yes, Sbo Hearing A/S’s devices are designed to be compatible with major hearing aid brands such as Oticon, Philips, and EarQ. Their product line includes accessories like wireless-fitting software, remote controls, and battery chargers that enhance functionality for these branded systems, ensuring seamless integration and user experience.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Denmark
- Address
- 9, Kongebakken, Smørum , Denmark
- Website
- www.demant.com
- —
- —
- [email protected]
- Phone
- +45 3917 7100
- PRRC Contact
- Susanne Bach Schmidt
- EUDAMED SRN
- DK-MF-000001270
- FDA FEI Number
- —
- DUNS Number
- 306018410
Catalogue (7857)
Page 15 of 158| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| EarQ | 259625 | FDA UDI | Class II | Active |
| Oticon | 270127 | FDA UDI | Class II | Active |
| Agxo | 258574 | FDA UDI | Class II | Active |
| Philips | 228218 | FDA UDI | Class II | Active |
| Oticon | 270128 | FDA UDI | Class II | Active |
| Philips | 237671 | FDA UDI | Class II | Active |
| Sonic | 238445 | FDA UDI | Class II | Active |
| Oticon | 268465 | FDA UDI | Class II | Active |
| Soniton | 277532 | FDA UDI | Class II | Active |
| Philips | 242487 | FDA UDI | Class II | Active |
| Oticon | 248627 | FDA UDI | Class II | Active |
| Sonic | 265709 | FDA UDI | Class II | Active |
| Agxo | 269754 | FDA UDI | Class II | Active |
| Oticon | 229093 | FDA UDI | Class II | Active |
| Oticon | 220336 | FDA UDI | Class II | Active |
| Philips | 196638 | FDA UDI | Class II | Active |
| Philips | 215393 | FDA UDI | Class II | Active |
| Oticon | 277531 | FDA UDI | Class II | Active |
| Philips | 264999 | FDA UDI | Class II | Active |
| Philips | 264989 | FDA UDI | Class II | Active |
| Philips | 268446 | FDA UDI | Class II | Active |
| Oticon | 214812 | FDA UDI | Class II | Active |
| Oticon | 270562 | FDA UDI | Class II | Active |
| Philips | 237674 | FDA UDI | Class II | Active |
| Philips | 215421 | FDA UDI | Class II | Active |
| Philips | 269927 | FDA UDI | Class II | Active |
| Oticon | 258485 | FDA UDI | Class II | Active |
| Oticon | 276159 | FDA UDI | Class II | Active |
| Bernafon | 247387 | FDA UDI | Class II | Active |
| Oticon | 241198 | FDA UDI | Class II | Active |
| Bernafon | 214982 | FDA UDI | Class II | Active |
| Bernafon | 269351 | FDA UDI | Class II | Active |
| Oticon | 255283 | FDA UDI | Class II | Active |
| Oticon | 270167 | FDA UDI | Class II | Active |
| Philips | 196605 | FDA UDI | Class II | Active |
| Bernafon | 262924 | FDA UDI | Class II | Active |
| EarQ | 259618 | FDA UDI | Class II | Active |
| Sonic | 238448 | FDA UDI | Class II | Active |
| Philips | 214709 | FDA UDI | Class II | Active |
| Oticon | 248184 | FDA UDI | Class II | Active |
| Philips | 197677 | FDA UDI | Class II | Active |
| Philips | 229400 | FDA UDI | Class II | Active |
| Oticon | 228229 | FDA UDI | Class II | Active |
| Philips | 196600 | FDA UDI | Class II | Active |
| Oticon | 270550 | FDA UDI | Class II | Active |
| Bernafon | 231715 | FDA UDI | Class II | Active |
| EarQ | 259608 | FDA UDI | Class II | Active |
| Oticon | 241149 | FDA UDI | Class II | Active |
| EarQ | 259613 | FDA UDI | Class II | Active |
| Sonic | 234777 | FDA UDI | Class II | Active |
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