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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 136 of 154
DeviceModel / ReferenceRegistriesClassStatus
Hhm 115288
FDA UDI
Class IIActive
Hhm 216005
FDA UDI
Class IIActive
Agxo 150137
FDA UDI
Class IIActive
Oticon 126164
FDA UDI
Class IIActive
Agxo 168307
FDA UDI
Class IIActive
Oticon 129884
FDA UDI
Class IIActive
Oticon 101387
FDA UDI
Class IIActive
Hhm 101531
FDA UDI
Class IIActive
Oticon 103-38-106-00
FDA UDI
Class IIActive
Oticon 191452
FDA UDI
Class IIActive
Oticon 632-01-507-00
FDA UDI
Class IIActive
Reveal 193502
FDA UDI
Class IIActive
EarQ 174936
FDA UDI
Class IIActive
Agxo 126427
FDA UDI
Class IIActive
EarQ 201610
FDA UDI
Class IIActive
Oticon 147119
FDA UDI
Class IIActive
Oticon 101668
FDA UDI
Class IIActive
Hhm 118711
FDA UDI
Class IIActive
Oticon 176035
FDA UDI
Class IIActive
Oticon 171140
FDA UDI
Class IIActive
Hhm 119537
FDA UDI
Class IIActive
Oticon 182599
FDA UDI
Class IIActive
Oticon 113529
FDA UDI
Class IActive
Oticon 207038
FDA UDI
Class IIActive
Oticon 150044
FDA UDI
Class IIActive
Oticon 155876
FDA UDI
Class IIActive
Oticon 146970
FDA UDI
Class IIActive
Oticon 150068
FDA UDI
Class IIActive
Agxo 149254
FDA UDI
Class IIActive
Oticon 157443
FDA UDI
Class IIActive
Oticon 103-42-200-00
FDA UDI
Class IIActive
Agxo 216100
FDA UDI
Class IIActive
Hhm 201678
FDA UDI
Class IIActive
Oticon 206998
FDA UDI
Class IIActive
Oticon 150043
FDA UDI
Class IIActive
Oticon 144477
FDA UDI
Class IIActive
Oticon 147221
FDA UDI
Class IActive
EarQ 201578
FDA UDI
Class IIActive
Oticon 103-40-107-00
FDA UDI
Class IIActive
Oticon 115111
FDA UDI
Class IActive
Oticon 155053
FDA UDI
Class IIActive
Oticon 108939
FDA UDI
Class IIActive
Oticon 150123
FDA UDI
Class IIActive
Oticon 150238
FDA UDI
Class IIActive
Oticon 146353
FDA UDI
Class IIActive
Oticon 150990
FDA UDI
Class IIActive
Hhm 193302
FDA UDI
Class IIActive
Agxo 150759
FDA UDI
Class IIActive
Agxo 133522
FDA UDI
Class IIActive
Oticon 188311
FDA UDI
Class IIActive

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