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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 125 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 129908
FDA UDI
Class IIActive
Oticon 126401
FDA UDI
Class IIActive
Agxo 119578
FDA UDI
Class IIActive
Oticon 115168
FDA UDI
Class IIActive
Oticon 175668
FDA UDI
Class IIActive
Hhm 168449
FDA UDI
Class IIActive
Hhm 201025
FDA UDI
Class IIActive
Agxo 174902
FDA UDI
Class IIActive
Agxo 155207
FDA UDI
Class IIActive
Agxo 103-24-182-00
FDA UDI
Class IIActive
Oticon 104742
FDA UDI
Class IIActive
Oticon 214960
FDA UDI
Class IIActive
Oticon 147045
FDA UDI
Class IIActive
Oticon 102-70-320-00
FDA UDI
Class IActive
Agxo 151178
FDA UDI
Class IIActive
Oticon 108983
FDA UDI
Class IIActive
EarQ 177343
FDA UDI
Class IIActive
Oticon 155865
FDA UDI
Class IIActive
Oticon 147092
FDA UDI
Class IActive
Oticon 144666
FDA UDI
Class IIActive
Oticon 147006
FDA UDI
Class IIActive
Hhm 201770
FDA UDI
Class IIActive
Oticon 212479
FDA UDI
Class IIActive
Oticon 150242
FDA UDI
Class IIActive
Agxo 193535
FDA UDI
Class IIActive
Oticon 205548
FDA UDI
Class IIActive
Oticon 190465
FDA UDI
Class IIActive
Oticon 131653
FDA UDI
Class IIActive
Oticon 118693
FDA UDI
Class IIActive
Hhm 118895
FDA UDI
Class IActive
Oticon 101932
FDA UDI
Class IIActive
Oticon 101548
FDA UDI
Class IIActive
Oticon 100647
FDA UDI
Class IIActive
Oticon 104-38-402-00
FDA UDI
Class IIActive
Oticon 175744
FDA UDI
Class IIActive
Oticon 147170
FDA UDI
Class IIActive
Agxo 162826
FDA UDI
Class IIActive
Oticon 115174
FDA UDI
Class IIActive
Bernafon 131233
FDA UDI
Class IIActive
Oticon 133250
FDA UDI
Class IIActive
Hhm 125617
FDA UDI
Class IIActive
Hhm 151169
FDA UDI
Class IIActive
Oticon 103-38-604-00
FDA UDI
Class IIActive
Oticon 102-01-402-00
FDA UDI
Class IActive
Oticon 103-23-406-00
FDA UDI
Class IIActive
Agxo 155965
FDA UDI
Class IIActive
Oticon 104-38-104-00
FDA UDI
Class IIActive
Agxo 150246
FDA UDI
Class IIActive
Oticon 147226
FDA UDI
Class IIActive
Oticon 150841
FDA UDI
Class IIActive

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