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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 129 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 149283
FDA UDI
Class IIActive
Oticon 226568
FDA UDI
Class IIActive
Oticon 178945
FDA UDI
Class IIActive
Oticon 150265
FDA UDI
Class IIActive
Oticon 149234
FDA UDI
Class IIActive
Agxo 177245
FDA UDI
Class IIActive
Oticon 132039
FDA UDI
Class IIActive
Agxo 126501
FDA UDI
Class IIActive
Agxo 149437
FDA UDI
Class IIActive
Agxo 108998
FDA UDI
Class IIActive
Oticon 196704
FDA UDI
Class IIActive
Hhm 150234
FDA UDI
Class IIActive
Oticon 133260
FDA UDI
Class IIActive
Oticon 108961
FDA UDI
Class IIActive
Hhm 103-39-024-00
FDA UDI
Class IIActive
Oticon 184276
FDA UDI
Class IIActive
Oticon 109436
FDA UDI
Class IActive
Oticon 102-76-204-00
FDA UDI
Class IActive
Oticon 146185
FDA UDI
Class IIActive
Oticon 191912
FDA UDI
Class IIActive
Oticon 150328
FDA UDI
Class IIActive
Oticon 127919
FDA UDI
Class IActive
Hhm 155879
FDA UDI
Class IIActive
Oticon 209288
FDA UDI
Class IIActive
Oticon 196684
FDA UDI
Class IIActive
Oticon 206970
FDA UDI
Class IIActive
Oticon 196788
FDA UDI
Class IIActive
Oticon 147200
FDA UDI
Class IActive
Oticon 118900
FDA UDI
Class IActive
Hhm 150822
FDA UDI
Class IIActive
Oticon 133823
FDA UDI
Class IIActive
Agxo 153768
FDA UDI
Class IIActive
Oticon 149168
FDA UDI
Class IIActive
Oticon 196786
FDA UDI
Class IIActive
Oticon 144492
FDA UDI
Class IIActive
Oticon 196685
FDA UDI
Class IIActive
Oticon 132330
FDA UDI
Class IIActive
Hhm 133362
FDA UDI
Class IIActive
Oticon 104-02-223-00
FDA UDI
Class IActive
EarQ 193564
FDA UDI
Class IIActive
Oticon 101390
FDA UDI
Class IIActive
Oticon 115184
FDA UDI
Class IIActive
Oticon 196681
FDA UDI
Class IIActive
Agxo 201300
FDA UDI
Class IIActive
Oticon 179501
FDA UDI
Class IIActive
Oticon 103-36-106-00
FDA UDI
Class IIActive
Oticon 109043
FDA UDI
Class IActive
Oticon 182618
FDA UDI
Class IIActive
Oticon 190461
FDA UDI
Class IIActive
Oticon 100717
FDA UDI
Class IIActive

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