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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 106 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 116227
FDA UDI
Class IIActive
Oticon 100684
FDA UDI
Class IIActive
Oticon 162482
FDA UDI
Class IIActive
Agxo 201344
FDA UDI
Class IIActive
Oticon 153210
FDA UDI
Class IIActive
Oticon 133780
FDA UDI
Class IActive
Oticon 100510
FDA UDI
Class IIActive
Hhm 133497
FDA UDI
Class IIActive
Agxo 126141
FDA UDI
Class IIActive
Oticon 104736
FDA UDI
Class IIActive
Oticon 149104
FDA UDI
Class IIActive
Oticon 133259
FDA UDI
Class IIActive
Agxo 133399
FDA UDI
Class IIActive
Oticon 100697
FDA UDI
Class IIActive
Oticon 124593
FDA UDI
Class IIActive
Agxo 115257
FDA UDI
Class IIActive
Oticon 157423
FDA UDI
Class IIActive
EarQ 193372
FDA UDI
Class IIActive
Agxo 176041
FDA UDI
Class IIActive
Hhm 115315
FDA UDI
Class IIActive
Hhm 101527
FDA UDI
Class IIActive
EarQ 201541
FDA UDI
Class IIActive
Hhm 193529
FDA UDI
Class IIActive
Oticon 140474
FDA UDI
Class IIActive
Oticon 101540
FDA UDI
Class IIActive
Oticon 101439
FDA UDI
Class IIActive
Oticon 108827
FDA UDI
Class IIActive
Oticon 108938
FDA UDI
Class IIActive
Oticon 102513
FDA UDI
Class IActive
Oticon 104-38-204-00
FDA UDI
Class IIActive
Agxo 174887
FDA UDI
Class IIActive
Oticon 214941
FDA UDI
Class IIActive
Oticon 205582
FDA UDI
Class IIActive
Oticon 147144
FDA UDI
Class IIActive
Oticon 103-40-309-00
FDA UDI
Class IIActive
Oticon 102780
FDA UDI
Class IActive
Oticon 197118
FDA UDI
Class IIActive
Agxo 216092
FDA UDI
Class IIActive
Hhm 151271
FDA UDI
Class IIActive
Oticon 131757
FDA UDI
Class IIActive
Agxo 151007
FDA UDI
Class IIActive
Agxo 151297
FDA UDI
Class IIActive
Oticon 103395
FDA UDI
Class IActive
Hhm 216012
FDA UDI
Class IIActive
Hhm 150108
FDA UDI
Class IIActive
Agxo 108954
FDA UDI
Class IIActive
Oticon 149172
FDA UDI
Class IIActive
Hhm 148974
FDA UDI
Class IIActive
Oticon 188312
FDA UDI
Class IIActive
Agxo 132472
FDA UDI
Class IIActive

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