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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 124 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 157419
FDA UDI
Class IIActive
Oticon 191968
FDA UDI
Class IIActive
Agxo 140431
FDA UDI
Class IIActive
Oticon 126179
FDA UDI
Class IActive
Oticon 116946
FDA UDI
Class IIActive
Oticon 104-38-202-00
FDA UDI
Class IIActive
Oticon 103-36-400-00
FDA UDI
Class IIActive
Oticon 157777
FDA UDI
Class IIActive
Oticon 108880
FDA UDI
Class IIActive
Oticon 191918
FDA UDI
Class IIActive
Oticon 104485
FDA UDI
Class IIActive
Hhm 149086
FDA UDI
Class IIActive
Reveal 177316
FDA UDI
Class IIActive
Oticon 153673
FDA UDI
Class IIActive
Oticon 207000
FDA UDI
Class IIActive
Oticon 112700
FDA UDI
Class IActive
Agxo 149374
FDA UDI
Class IIActive
Hhm 150155
FDA UDI
Class IIActive
Oticon 133463
FDA UDI
Class IIActive
Oticon 216029
FDA UDI
Class IIActive
Oticon 177035
FDA UDI
Class IIActive
Hhm 132450
FDA UDI
Class IIActive
Oticon 197100
FDA UDI
Class IIActive
Agxo 151278
FDA UDI
Class IIActive
Oticon 109038
FDA UDI
Class IIActive
Oticon 147186
FDA UDI
Class IIActive
Hhm 149163
FDA UDI
Class IIActive
Oticon 133856
FDA UDI
Class IActive
Hhm 132367
FDA UDI
Class IIActive
Oticon 147063
FDA UDI
Class IIActive
Oticon 114521
FDA UDI
Class IIActive
Agxo 103-37-281-00
FDA UDI
Class IIActive
Oticon 104-02-421-00
FDA UDI
Class IActive
Oticon 103-40-208-00
FDA UDI
Class IIActive
Oticon 182587
FDA UDI
Class IIActive
Hhm 133495
FDA UDI
Class IIActive
Agxo 119518
FDA UDI
Class IIActive
Oticon 104-23-104-00
FDA UDI
Class IIActive
Oticon 149599
FDA UDI
Class IIActive
Oticon 151253
FDA UDI
Class IIActive
Agxo 150202
FDA UDI
Class IIActive
Oticon 188323
FDA UDI
Class IIActive
Hhm 201784
FDA UDI
Class IIActive
Agxo 132428
FDA UDI
Class IIActive
EarQ 201574
FDA UDI
Class IIActive
Oticon 193727
FDA UDI
Class IIActive
Agxo 118904
FDA UDI
Class IActive
Oticon 115155
FDA UDI
Class IIActive
Agxo 126506
FDA UDI
Class IIActive
Oticon 106-24-310-10
FDA UDI
Class IActive

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