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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 41 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 133210
FDA UDI
Class IIActive
EarQ 174948
FDA UDI
Class IIActive
Hhm 103-24-021-00
FDA UDI
Class IIActive
Oticon 187492
FDA UDI
Class IIActive
Agxo 108951
FDA UDI
Class IIActive
Oticon 100784
FDA UDI
Class IIActive
Oticon 114579
FDA UDI
Class IIActive
Hhm 101450
FDA UDI
Class IIActive
Hhm 149087
FDA UDI
Class IIActive
Hhm 113331
FDA UDI
Class IActive
Oticon 125977
FDA UDI
Class IIActive
Oticon 155931
FDA UDI
Class IIActive
Oticon 103-38-409-00
FDA UDI
Class IIActive
Agxo 151318
FDA UDI
Class IIActive
Hhm 108846
FDA UDI
Class IIActive
Oticon 109435
FDA UDI
Class IActive
Oticon 206617
FDA UDI
Class IIActive
Hhm 201009
FDA UDI
Class IIActive
Hhm 168448
FDA UDI
Class IIActive
Oticon 106-29-660-10
FDA UDI
Class IIActive
Oticon 133341
FDA UDI
Class IIActive
Oticon 182773
FDA UDI
Class IIActive
Hhm 133415
FDA UDI
Class IIActive
Oticon 119613
FDA UDI
Class IIActive
Oticon 206977
FDA UDI
Class IIActive
Oticon 147175
FDA UDI
Class IIActive
Oticon 101568
FDA UDI
Class IActive
Oticon 101850
FDA UDI
Class IIActive
Hhm 104-37-231-00
FDA UDI
Class IIActive
Hhm 125614
FDA UDI
Class IIActive
Hhm 103-24-324-00
FDA UDI
Class IIActive
Oticon 146976
FDA UDI
Class IIActive
Oticon 150404
FDA UDI
Class IIActive
Hhm 140263
FDA UDI
Class IIActive
Oticon 214944
FDA UDI
Class IIActive
Oticon 150452
FDA UDI
Class IIActive
Oticon 157502
FDA UDI
Class IIActive
Oticon 109011
FDA UDI
Class IActive
Hhm 174877
FDA UDI
Class IIActive
Agxo 150395
FDA UDI
Class IIActive
Oticon 148998
FDA UDI
Class IIActive
Oticon 150707
FDA UDI
Class IIActive
Oticon 205574
FDA UDI
Class IIActive
Oticon 147222
FDA UDI
Class IIActive
Agxo 132474
FDA UDI
Class IIActive
Oticon 118741
FDA UDI
Class IIActive
Agxo 155205
FDA UDI
Class IIActive
Agxo 151300
FDA UDI
Class IIActive
Oticon 157473
FDA UDI
Class IIActive
Oticon 109433
FDA UDI
Class IActive

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