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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 137 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 131790
FDA UDI
Class IIActive
Agxo 118674
FDA UDI
Class IIActive
Oticon 150953
FDA UDI
Class IIActive
Oticon 140467
FDA UDI
Class IIActive
Oticon 100706
FDA UDI
Class IIActive
Oticon 208859
FDA UDI
Class IIActive
Reveal 193507
FDA UDI
Class IIActive
Agxo 201345
FDA UDI
Class IIActive
Oticon 188316
FDA UDI
Class IIActive
Oticon 182760
FDA UDI
Class IIActive
Oticon 153212
FDA UDI
Class IIActive
Oticon 131656
FDA UDI
Class IIActive
Agxo 103062
FDA UDI
Class IIActive
Oticon 104-38-910-00
FDA UDI
Class IIActive
Agxo 201333
FDA UDI
Class IIActive
Oticon 150961
FDA UDI
Class IIActive
Oticon 104-23-401-00
FDA UDI
Class IIActive
Oticon 103-38-403-00
FDA UDI
Class IIActive
Oticon 135315
FDA UDI
Class IIActive
Oticon 115158
FDA UDI
Class IIActive
Oticon 101384
FDA UDI
Class IIActive
Hhm 216044
FDA UDI
Class IIActive
EarQ 201573
FDA UDI
Class IIActive
Hhm 201783
FDA UDI
Class IIActive
Agxo 193534
FDA UDI
Class IIActive
Oticon 150704
FDA UDI
Class IIActive
Oticon 144490
FDA UDI
Class IIActive
Hhm 118508
FDA UDI
Class IIActive
Oticon 103405
FDA UDI
Class IActive
EarQ 201543
FDA UDI
Class IIActive
Oticon 115183
FDA UDI
Class IIActive
Oticon 141630
FDA UDI
Class IIActive
Agxo 174891
FDA UDI
Class IIActive
Oticon 103-23-011-00
FDA UDI
Class IIActive
Oticon 106-61-240-10
FDA UDI
Class IIActive
Oticon 140481
FDA UDI
Class IIActive
Hhm 115310
FDA UDI
Class IIActive
Oticon 155200
FDA UDI
Class IIActive
Oticon 104-38-208-00
FDA UDI
Class IIActive
Oticon 103-38-505-00
FDA UDI
Class IIActive
Agxo 133477
FDA UDI
Class IIActive
Oticon 115169
FDA UDI
Class IIActive
Oticon 191958
FDA UDI
Class IIActive
Oticon 113146
FDA UDI
Class IActive
Agxo 119565
FDA UDI
Class IIActive
Hhm 158440
FDA UDI
Class IIActive
Oticon 206969
FDA UDI
Class IIActive
Oticon 133464
FDA UDI
Class IIActive
Oticon 113481
FDA UDI
Class IActive
Oticon 196812
FDA UDI
Class IIActive

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