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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 29 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 106-24-230-10
FDA UDI
Class IIActive
Agxo 104-24-582-00
FDA UDI
Class IIActive
Agxo 133430
FDA UDI
Class IIActive
Oticon 182725
FDA UDI
Class IIActive
Oticon 103-42-301-00
FDA UDI
Class IIActive
Oticon 161432
FDA UDI
Class IIActive
Oticon 116947
FDA UDI
Class IIActive
Oticon 104-23-501-00
FDA UDI
Class IIActive
Oticon 104-02-483-00
FDA UDI
Class IActive
Oticon 103-36-604-00
FDA UDI
Class IIActive
Oticon 182576
FDA UDI
Class IIActive
Hhm 116403
FDA UDI
Class IIActive
Hhm 193295
FDA UDI
Class IIActive
Hhm 174865
FDA UDI
Class IIActive
Oticon 100040
FDA UDI
Class IIActive
Oticon 103-24-351-00
FDA UDI
Class IIActive
Oticon 102-76-103-00
FDA UDI
Class IActive
Oticon 197333
FDA UDI
Class IIActive
Oticon 146339
FDA UDI
Class IIActive
Hhm 149079
FDA UDI
Class IIActive
EarQ 177334
FDA UDI
Class IIActive
Oticon 147013
FDA UDI
Class IActive
Oticon 150039
FDA UDI
Class IIActive
Oticon 148995
FDA UDI
Class IIActive
Oticon 136943
FDA UDI
Class IIActive
Agxo 103624
FDA UDI
Class IIActive
Reveal 177300
FDA UDI
Class IIActive
Oticon 197113
FDA UDI
Class IIActive
Oticon 176649
FDA UDI
Class IIActive
Oticon 196768
FDA UDI
Class IIActive
Agxo 151280
FDA UDI
Class IIActive
EarQ 193566
FDA UDI
Class IIActive
Oticon 147159
FDA UDI
Class IIActive
Agxo 115253
FDA UDI
Class IIActive
Agxo 149114
FDA UDI
Class IIActive
Reveal 193390
FDA UDI
Class IIActive
Hhm 103-37-769-00
FDA UDI
Class IIActive
Oticon 212475
FDA UDI
Class IIActive
Oticon 149517
FDA UDI
Class IIActive
Oticon 149174
FDA UDI
Class IIActive
Oticon 131216
FDA UDI
Class IIActive
Oticon 108923
FDA UDI
Class IIActive
Oticon 207990
FDA UDI
Class IIActive
Hhm 149224
FDA UDI
Class IIActive
Oticon 132337
FDA UDI
Class IIActive
Reveal 193503
FDA UDI
Class IIActive
Oticon 133376
FDA UDI
Class IIActive
Oticon 207064
FDA UDI
Class IIActive
Oticon 131793
FDA UDI
Class IIActive
Hhm 201014
FDA UDI
Class IIActive

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