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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 140 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 103-42-102-00
FDA UDI
Class IIActive
Oticon 108902
FDA UDI
Class IIActive
Oticon 150065
FDA UDI
Class IIActive
Oticon 114207
FDA UDI
Class IIActive
Hhm 104-39-433-00
FDA UDI
Class IIActive
Oticon 191889
FDA UDI
Class IIActive
Oticon 205547
FDA UDI
Class IIActive
Hhm 150976
FDA UDI
Class IIActive
Agxo 149370
FDA UDI
Class IIActive
Agxo 148973
FDA UDI
Class IIActive
Oticon 209223
FDA UDI
Class IIActive
Oticon 191894
FDA UDI
Class IIActive
Agxo 151048
FDA UDI
Class IIActive
EarQ 176098
FDA UDI
Class IIActive
Hhm 201682
FDA UDI
Class IIActive
Hhm 133501
FDA UDI
Class IIActive
Reveal 193402
FDA UDI
Class IIActive
Oticon 124965
FDA UDI
Class IIActive
Oticon 114591
FDA UDI
Class IIActive
Agxo 126139
FDA UDI
Class IIActive
Oticon 121731
FDA UDI
Class IIActive
Hhm 103-24-320-00
FDA UDI
Class IIActive
Oticon 216026
FDA UDI
Class IIActive
Oticon 104493
FDA UDI
Class IIActive
Oticon 131747
FDA UDI
Class IIActive
Oticon 146362
FDA UDI
Class IIActive
Oticon 157795
FDA UDI
Class IIActive
Oticon 193731
FDA UDI
Class IIActive
Oticon 114108
FDA UDI
Class IIActive
Agxo 108992
FDA UDI
Class IIActive
Oticon 106-31-660-10
FDA UDI
Class IIActive
Hhm 201071
FDA UDI
Class IIActive
Oticon 150079
FDA UDI
Class IIActive
Agxo 148970
FDA UDI
Class IIActive
Oticon 118750
FDA UDI
Class IIActive
Hhm 158452
FDA UDI
Class IIActive
Agxo 133348
FDA UDI
Class IIActive
Oticon 115188
FDA UDI
Class IIActive
Hhm 115323
FDA UDI
Class IIActive
Hhm 103-24-124-00
FDA UDI
Class IIActive
Oticon 106-29-260-10
FDA UDI
Class IIActive
Hhm 133499
FDA UDI
Class IIActive
EarQ 174954
FDA UDI
Class IIActive
Oticon 150059
FDA UDI
Class IIActive
Oticon 196808
FDA UDI
Class IIActive
Hhm 150740
FDA UDI
Class IIActive
Oticon 102774
FDA UDI
Class IActive
Agxo 201352
FDA UDI
Class IIActive
Oticon 176602
FDA UDI
Class IIActive
Oticon 150681
FDA UDI
Class IIActive

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