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Oticon A/S

US

Last updated May 24, 2026

What Oticon A/S makes

Oticon A/S manufactures a range of air-conduction hearing aids, including receiver-in-the-ear, behind-the-ear, in-the-ear, and canal models. Their portfolio also includes audiometric/hearing device software, wireless-fitting computer-aided systems, remote controls for hearing aids, and wireless induction loops for hearing aid users.

The company’s devices are classified under FDA categories Class I and Class II, with products listed in the FDA’s Unique Device Identifier (UDI) database. Oticon A/S is based in the United States.

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 Oticon A/S manufacture?

Oticon A/S specializes in air-conduction hearing aids, covering multiple form factors such as receiver-in-the-ear, behind-the-ear, in-the-ear, and canal models. Their portfolio also includes audiometric/hearing device software, wireless-fitting computer-aided systems, remote controls for hearing aids, and wireless induction loops designed to assist hearing aid users. These devices are developed to address various hearing loss needs and improve auditory access.

Where is Oticon A/S based, and does it operate internationally?

Oticon A/S is headquartered in the United States. While the company’s primary location is in the US, its devices are designed to meet global regulatory standards, including those in the FDA’s Unique Device Identifier (UDI) database. The company’s focus on hearing solutions suggests a broad market reach, though specific international operations or subsidiaries are not detailed in the available data.

Which regulatory registries list Oticon A/S’s devices?

Oticon A/S’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to track and identify medical devices in the United States, ensuring transparency and traceability for regulatory and market surveillance purposes. This listing applies to their air-conduction hearing aids and related accessories, as categorized under Class I and Class II devices.

How are Oticon A/S’s hearing aids classified by the FDA?

Oticon A/S’s hearing aids fall under two FDA device classes: Class I and Class II. Class I generally includes low-risk devices that pose minimal potential harm, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and benefits, as determined by regulatory authorities like the FDA.

What distinguishes Oticon A/S’s wireless-fitting computer-aided systems from other hearing aid technologies?

Oticon A/S’s wireless-fitting computer-aided systems are designed to streamline the customization and programming of hearing aids, enabling audiologists to adjust settings remotely and efficiently. These systems integrate with their air-conduction hearing aids to enhance fitting accuracy, user experience, and connectivity—such as pairing with smartphones or other devices—thereby improving accessibility and personalization for hearing aid users. This approach aligns with modern trends toward digital and wireless solutions in audiology.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
oticon.com
LinkedIn
—
Facebook
—
Phone
+4539177100
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
305839946

Catalogue (7693)

Page 139 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 104731
FDA UDI
Class IIActive
Oticon 101543
FDA UDI
Class IIActive
Agxo 103216
FDA UDI
Class IIActive
Agxo 126424
FDA UDI
Class IIActive
Agxo 119573
FDA UDI
Class IIActive
Oticon 205526
FDA UDI
Class IIActive
Hhm 150731
FDA UDI
Class IIActive
Agxo 115280
FDA UDI
Class IIActive
Hhm 101361
FDA UDI
Class IIActive
Hhm 126481
FDA UDI
Class IIActive
Oticon 133465
FDA UDI
Class IIActive
Oticon 155846
FDA UDI
Class IIActive
Oticon 114576
FDA UDI
Class IIActive
Oticon 100678
FDA UDI
Class IIActive
Oticon 102618
FDA UDI
Class IIActive
Oticon 104-23-505-00
FDA UDI
Class IIActive
Oticon 103-36-015-00
FDA UDI
Class IIActive
Oticon 146992
FDA UDI
Class IIActive
Agxo 193308
FDA UDI
Class IIActive
Hhm 201072
FDA UDI
Class IIActive
Oticon 150867
FDA UDI
Class IIActive
Oticon 130961
FDA UDI
Class IIActive
Agxo 103619
FDA UDI
Class IIActive
Oticon 147184
FDA UDI
Class IIActive
Oticon 133471
FDA UDI
Class IIActive
Agxo 126419
FDA UDI
Class IIActive
Hhm 150979
FDA UDI
Class IIActive
Oticon 161422
FDA UDI
Class IIActive
Agxo 140423
FDA UDI
Class IIActive
Oticon 102-76-110-00
FDA UDI
Class IActive
EarQ 201553
FDA UDI
Class IIActive
Oticon 146996
FDA UDI
Class IIActive
Oticon 103-36-013-00
FDA UDI
Class IIActive
Oticon 114211
FDA UDI
Class IIActive
Oticon 146275
FDA UDI
Class IIActive
Oticon 137407
FDA UDI
Class IActive
Oticon 109023
FDA UDI
Class IIActive
Agxo 108862
FDA UDI
Class IIActive
Oticon 104-23-406-00
FDA UDI
Class IIActive
Oticon 186558
FDA UDI
Class IIActive
Oticon 132282
FDA UDI
Class IIActive
Oticon 161822
FDA UDI
Class IIActive
Oticon 198482
FDA UDI
Class IIActive
Agxo 151898
FDA UDI
Class IIActive
EarQ 216220
FDA UDI
Class IIActive
Oticon 109424
FDA UDI
Class IActive
Oticon 146174
FDA UDI
Class IIActive
Agxo 132346
FDA UDI
Class IIActive
Agxo 155963
FDA UDI
Class IIActive
Oticon 100767
FDA UDI
Class IActive

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