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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 34 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 126125
FDA UDI
Class IIActive
Hhm 201728
FDA UDI
Class IIActive
Hhm 101421
FDA UDI
Class IIActive
Agxo 104-24-581-00
FDA UDI
Class IIActive
Oticon 106-23-280-10
FDA UDI
Class IActive
Oticon 114107
FDA UDI
Class IIActive
Hhm 151170
FDA UDI
Class IIActive
Oticon 104-02-322-00
FDA UDI
Class IActive
Oticon 109059
FDA UDI
Class IActive
Oticon 140463
FDA UDI
Class IIActive
Oticon 108852
FDA UDI
Class IIActive
Oticon 183832
FDA UDI
Class IIActive
Oticon 191946
FDA UDI
Class IIActive
Oticon 104-38-102-00
FDA UDI
Class IIActive
Oticon 205362
FDA UDI
Class IIActive
Oticon 103-36-930-00
FDA UDI
Class IIActive
Oticon 100641
FDA UDI
Class IIActive
Oticon 137831
FDA UDI
Class IIActive
Oticon 212477
FDA UDI
Class IIActive
Oticon 150240
FDA UDI
Class IIActive
Oticon 191955
FDA UDI
Class IIActive
Oticon 151258
FDA UDI
Class IIActive
Oticon 150220
FDA UDI
Class IIActive
Oticon 150023
FDA UDI
Class IIActive
Agxo 151052
FDA UDI
Class IIActive
Oticon 126186
FDA UDI
Class IActive
Oticon 103-38-506-00
FDA UDI
Class IIActive
Oticon 106-61-600-10
FDA UDI
Class IIActive
Oticon 186570
FDA UDI
Class IIActive
Oticon 205552
FDA UDI
Class IIActive
EarQ 201618
FDA UDI
Class IIActive
Oticon 133170
FDA UDI
Class IIActive
Hhm 193291
FDA UDI
Class IIActive
Oticon 197335
FDA UDI
Class IIActive
Hhm 101535
FDA UDI
Class IIActive
Oticon 196800
FDA UDI
Class IIActive
Agxo 132384
FDA UDI
Class IIActive
Oticon 109033
FDA UDI
Class IActive
Oticon 147143
FDA UDI
Class IIActive
Hhm 132325
FDA UDI
Class IIActive
Agxo 150139
FDA UDI
Class IIActive
Hhm 149510
FDA UDI
Class IIActive
Oticon 188342
FDA UDI
Class IIActive
Oticon 216037
FDA UDI
Class IIActive
Oticon 151646
FDA UDI
Class IIActive
Hhm 150113
FDA UDI
Class IIActive
Oticon 147164
FDA UDI
Class IIActive
Agxo 149373
FDA UDI
Class IIActive
Agxo 151057
FDA UDI
Class IIActive
Oticon 132331
FDA UDI
Class IIActive

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