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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 109 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 131199
FDA UDI
Class IIActive
Oticon 101897
FDA UDI
Class IIActive
Oticon 205591
FDA UDI
Class IIActive
Oticon 131853
FDA UDI
Class IActive
Oticon 118905
FDA UDI
Class IActive
Oticon 126120
FDA UDI
Class IIActive
Hhm 193294
FDA UDI
Class IIActive
Oticon 106-68-430-10
FDA UDI
Class IActive
Hhm 201752
FDA UDI
Class IIActive
Hhm 126346
FDA UDI
Class IIActive
EarQ 193571
FDA UDI
Class IIActive
Hhm 150363
FDA UDI
Class IIActive
Oticon 146271
FDA UDI
Class IIActive
Oticon 109019
FDA UDI
Class IIActive
Oticon 151184
FDA UDI
Class IIActive
Oticon 118606
FDA UDI
Class IIActive
Agxo 126325
FDA UDI
Class IIActive
Oticon 115138
FDA UDI
Class IIActive
Oticon 150310
FDA UDI
Class IIActive
Oticon 196672
FDA UDI
Class IIActive
Oticon 209271
FDA UDI
Class IIActive
Oticon 145989
FDA UDI
Class IIActive
Hhm 103-39-112-00
FDA UDI
Class IIActive
Hhm 132274
FDA UDI
Class IIActive
Hhm 103-37-212-00
FDA UDI
Class IIActive
Agxo 193317
FDA UDI
Class IIActive
Oticon 155197
FDA UDI
Class IIActive
Oticon 125141
FDA UDI
Class IActive
Oticon 106-23-440-10
FDA UDI
Class IIActive
Oticon 147044
FDA UDI
Class IIActive
Oticon 147106
FDA UDI
Class IActive
Oticon 132459
FDA UDI
Class IIActive
Oticon 133470
FDA UDI
Class IIActive
Oticon 204454
FDA UDI
Class IIActive
Hhm 103-24-322-00
FDA UDI
Class IIActive
Oticon 106-76-400-10
FDA UDI
Class IActive
Oticon 133417
FDA UDI
Class IIActive
Oticon 100712
FDA UDI
Class IIActive
Oticon 124594
FDA UDI
Class IIActive
Oticon 141627
FDA UDI
Class IIActive
Oticon 118695
FDA UDI
Class IIActive
Oticon 119616
FDA UDI
Class IIActive
Oticon 115016
FDA UDI
Class IIActive
Agxo 174899
FDA UDI
Class IIActive
Oticon 158601
FDA UDI
Class IIActive
Oticon 119553
FDA UDI
Class IIActive
Oticon 103-38-016-00
FDA UDI
Class IIActive
Oticon 225121
FDA UDI
Class IIActive
Hhm 158454
FDA UDI
Class IIActive
Agxo 177246
FDA UDI
Class IIActive

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