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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 22 of 154
DeviceModel / ReferenceRegistriesClassStatus
Claris 170467
FDA UDI
Class IIActive
Oticon 147141
FDA UDI
Class IIActive
Oticon 151033
FDA UDI
Class IIActive
Hhm 132324
FDA UDI
Class IIActive
Hhm 148977
FDA UDI
Class IIActive
Oticon 170137
FDA UDI
Class IIActive
Oticon 132295
FDA UDI
Class IIActive
Oticon 147087
FDA UDI
Class IIActive
Oticon 101545
FDA UDI
Class IIActive
Oticon 104-02-201-00
FDA UDI
Class IActive
Oticon 116225
FDA UDI
Class IIActive
Oticon 106-71-210-10
FDA UDI
Class IIActive
Oticon 115154
FDA UDI
Class IIActive
Oticon 141410
FDA UDI
Class IIActive
Oticon 104-02-302-00
FDA UDI
Class IActive
Oticon 114069
FDA UDI
Class IIActive
Oticon 114590
FDA UDI
Class IIActive
Oticon 191961
FDA UDI
Class IIActive
Reveal 193576
FDA UDI
Class IIActive
Agxo 201316
FDA UDI
Class IIActive
Agxo 176064
FDA UDI
Class IIActive
Oticon 118607
FDA UDI
Class IIActive
EarQ 201549
FDA UDI
Class IIActive
Hhm 201027
FDA UDI
Class IIActive
Oticon 150692
FDA UDI
Class IIActive
Oticon 133209
FDA UDI
Class IIActive
Oticon 119554
FDA UDI
Class IIActive
Hhm 118503
FDA UDI
Class IIActive
Oticon 147088
FDA UDI
Class IIActive
Oticon 147163
FDA UDI
Class IIActive
Oticon 118738
FDA UDI
Class IIActive
Hhm 104-39-130-00
FDA UDI
Class IIActive
Oticon 147089
FDA UDI
Class IIActive
Oticon 131220
FDA UDI
Class IIActive
Agxo 118678
FDA UDI
Class IIActive
Oticon 215030
FDA UDI
Class IIActive
Oticon 191450
FDA UDI
Class IIActive
Agxo 201284
FDA UDI
Class IIActive
Agxo 174901
FDA UDI
Class IIActive
Agxo 133528
FDA UDI
Class IIActive
Agxo 103-24-181-00
FDA UDI
Class IIActive
Oticon 126126
FDA UDI
Class IIActive
Oticon 100694
FDA UDI
Class IIActive
Oticon 103-36-406-00
FDA UDI
Class IIActive
Oticon 126123
FDA UDI
Class IIActive
Hhm 115311
FDA UDI
Class IIActive
Agxo 150455
FDA UDI
Class IIActive
Agxo 149523
FDA UDI
Class IIActive
Oticon 104-23-900-00
FDA UDI
Class IIActive
Oticon 147104
FDA UDI
Class IActive

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