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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 110 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 133262
FDA UDI
Class IIActive
Agxo 115281
FDA UDI
Class IIActive
Oticon 182619
FDA UDI
Class IIActive
Hhm 174875
FDA UDI
Class IIActive
Hhm 133372
FDA UDI
Class IIActive
Hhm 125616
FDA UDI
Class IIActive
Oticon 181631
FDA UDI
Class IIActive
Oticon 106-31-500-10
FDA UDI
Class IActive
Agxo 133355
FDA UDI
Class IIActive
Oticon 104747
FDA UDI
Class IIActive
Oticon 106-68-420-10
FDA UDI
Class IActive
Agxo 177229
FDA UDI
Class IIActive
Agxo 148971
FDA UDI
Class IIActive
Hhm 118714
FDA UDI
Class IIActive
Oticon 100709
FDA UDI
Class IIActive
Agxo 150136
FDA UDI
Class IIActive
Oticon 109432
FDA UDI
Class IActive
Oticon 151238
FDA UDI
Class IIActive
Oticon 104-24-264-00
FDA UDI
Class IIActive
Oticon 103-36-506-00
FDA UDI
Class IIActive
Oticon 161428
FDA UDI
Class IIActive
Hhm 150821
FDA UDI
Class IIActive
Oticon 202028
FDA UDI
Class IIActive
Oticon 131849
FDA UDI
Class IIActive
Oticon 147028
FDA UDI
Class IIActive
Oticon 106-29-610-10
FDA UDI
Class IIActive
Hhm 104-39-332-00
FDA UDI
Class IIActive
Oticon 178960
FDA UDI
Class IIActive
Oticon 103-40-307-00
FDA UDI
Class IIActive
Oticon 193881
FDA UDI
Class IIActive
EarQ 216236
FDA UDI
Class IIActive
Oticon 150243
FDA UDI
Class IIActive
Oticon 177085
FDA UDI
Class IIActive
Hhm 149508
FDA UDI
Class IIActive
Hhm 149158
FDA UDI
Class IIActive
Oticon 131874
FDA UDI
Class IIActive
Oticon 103-42-201-00
FDA UDI
Class IIActive
Oticon 155954
FDA UDI
Class IIActive
Oticon 214968
FDA UDI
Class IIActive
Oticon 182591
FDA UDI
Class IIActive
Oticon 131785
FDA UDI
Class IIActive
Hhm 201772
FDA UDI
Class IIActive
Hhm 118896
FDA UDI
Class IActive
Hhm 193458
FDA UDI
Class IIActive
Oticon 140475
FDA UDI
Class IIActive
Oticon 133252
FDA UDI
Class IIActive
Oticon 126315
FDA UDI
Class IIActive
Oticon 114548
FDA UDI
Class IIActive
Oticon 113485
FDA UDI
Class IActive
Hhm 216056
FDA UDI
Class IIActive

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