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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 12 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 103-38-304-00
FDA UDI
Class IIActive
Oticon 149096
FDA UDI
Class IIActive
Agxo 172117
FDA UDI
Class IIActive
Oticon 104-23-403-00
FDA UDI
Class IIActive
Oticon 109045
FDA UDI
Class IActive
Reveal 193572
FDA UDI
Class IIActive
Hhm 150782
FDA UDI
Class IIActive
Agxo 104-24-284-00
FDA UDI
Class IIActive
Oticon 125644
FDA UDI
Class IActive
Oticon 133214
FDA UDI
Class IIActive
Oticon 103-38-307-00
FDA UDI
Class IIActive
Oticon 150087
FDA UDI
Class IIActive
Oticon 103-40-108-00
FDA UDI
Class IIActive
Hhm 177226
FDA UDI
Class IIActive
Oticon 102076
FDA UDI
Class IIActive
Agxo 103060
FDA UDI
Class IIActive
Oticon 157472
FDA UDI
Class IIActive
Oticon 171158
FDA UDI
Class IIActive
Agxo 150415
FDA UDI
Class IIActive
Agxo 216065
FDA UDI
Class IIActive
Oticon 191919
FDA UDI
Class IIActive
Oticon 150266
FDA UDI
Class IIActive
Oticon 150067
FDA UDI
Class IIActive
Agxo 149108
FDA UDI
Class IIActive
Hhm 216051
FDA UDI
Class IIActive
Oticon 153880
FDA UDI
Class IIActive
Reveal 177293
FDA UDI
Class IIActive
Hhm 177200
FDA UDI
Class IIActive
Oticon 146348
FDA UDI
Class IIActive
Hhm 150187
FDA UDI
Class IIActive
Agxo 132434
FDA UDI
Class IIActive
Hhm 155886
FDA UDI
Class IIActive
Oticon 100646
FDA UDI
Class IIActive
Agxo 150810
FDA UDI
Class IIActive
Oticon 190462
FDA UDI
Class IIActive
Oticon 155961
FDA UDI
Class IIActive
Oticon 147215
FDA UDI
Class IIActive
Oticon 147062
FDA UDI
Class IIActive
Hhm 150777
FDA UDI
Class IIActive
Oticon 106-68-310-10
FDA UDI
Class IActive
Hhm 126479
FDA UDI
Class IIActive
Oticon 140038
FDA UDI
Class IIActive
Oticon 126154
FDA UDI
Class IIActive
Agxo 113342
FDA UDI
Class IActive
Agxo 155908
FDA UDI
Class IIActive
Oticon 103-38-930-00
FDA UDI
Class IIActive
Oticon 157418
FDA UDI
Class IIActive
Oticon 126182
FDA UDI
Class IActive
Agxo 174888
FDA UDI
Class IIActive
Oticon 108922
FDA UDI
Class IIActive

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