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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 43 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 150050
FDA UDI
Class IIActive
Oticon 191898
FDA UDI
Class IIActive
Oticon 206975
FDA UDI
Class IIActive
Oticon 146354
FDA UDI
Class IIActive
Oticon 131918
FDA UDI
Class IActive
Hhm 150210
FDA UDI
Class IIActive
Agxo 150457
FDA UDI
Class IIActive
Oticon 146035
FDA UDI
Class IIActive
Oticon 133174
FDA UDI
Class IIActive
Oticon 130962
FDA UDI
Class IIActive
Agxo 150248
FDA UDI
Class IIActive
Oticon 205568
FDA UDI
Class IIActive
Oticon 150329
FDA UDI
Class IIActive
Oticon 187780
FDA UDI
Class IIActive
Oticon 124820
FDA UDI
Class IIActive
Oticon 198607
FDA UDI
Class IIActive
Oticon 205539
FDA UDI
Class IIActive
Oticon 198600
FDA UDI
Class IIActive
Oticon 176557
FDA UDI
Class IIActive
Oticon 147112
FDA UDI
Class IIActive
Agxo 151004
FDA UDI
Class IIActive
Oticon 102507
FDA UDI
Class IActive
Oticon 131208
FDA UDI
Class IIActive
Oticon 205529
FDA UDI
Class IIActive
Oticon 150753
FDA UDI
Class IIActive
Oticon 151198
FDA UDI
Class IIActive
Agxo 201297
FDA UDI
Class IIActive
Hhm 201054
FDA UDI
Class IIActive
Hhm 201777
FDA UDI
Class IIActive
Oticon 196652
FDA UDI
Class IIActive
Hhm 148978
FDA UDI
Class IIActive
Oticon 191942
FDA UDI
Class IIActive
Oticon 125981
FDA UDI
Class IIActive
Oticon 155878
FDA UDI
Class IIActive
Oticon 102-76-190-00
FDA UDI
Class IActive
Oticon 131223
FDA UDI
Class IIActive
Hhm 177204
FDA UDI
Class IIActive
Oticon 175654
FDA UDI
Class IIActive
Oticon 108917
FDA UDI
Class IIActive
Oticon 125979
FDA UDI
Class IIActive
Oticon 193726
FDA UDI
Class IIActive
Agxo 193311
FDA UDI
Class IIActive
Oticon 191907
FDA UDI
Class IIActive
Oticon 132334
FDA UDI
Class IIActive
Agxo 103612
FDA UDI
Class IIActive
Oticon 150888
FDA UDI
Class IIActive
Oticon 177087
FDA UDI
Class IIActive
Oticon 146982
FDA UDI
Class IActive
Hhm 201047
FDA UDI
Class IIActive
Oticon 129843
FDA UDI
Class IIActive

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