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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 138 of 154
DeviceModel / ReferenceRegistriesClassStatus
Oticon 131883
FDA UDI
Class IActive
Oticon 157499
FDA UDI
Class IIActive
Oticon 147214
FDA UDI
Class IIActive
Oticon 147127
FDA UDI
Class IIActive
Hhm 150402
FDA UDI
Class IIActive
Oticon 140231
FDA UDI
Class IIActive
Agxo 126017
FDA UDI
Class IIActive
Agxo 126138
FDA UDI
Class IIActive
Oticon 132420
FDA UDI
Class IIActive
Oticon 178971
FDA UDI
Class IIActive
Agxo 149372
FDA UDI
Class IIActive
Oticon 182750
FDA UDI
Class IIActive
Oticon 125629
FDA UDI
Class IIActive
Oticon 103-42-101-00
FDA UDI
Class IIActive
Agxo 168306
FDA UDI
Class IIActive
Hhm 126478
FDA UDI
Class IIActive
Oticon 114545
FDA UDI
Class IIActive
Hhm 115318
FDA UDI
Class IIActive
Hhm 108146
FDA UDI
Class IIActive
Oticon 101386
FDA UDI
Class IIActive
Hhm 201038
FDA UDI
Class IIActive
Oticon 146166
FDA UDI
Class IIActive
Oticon 126163
FDA UDI
Class IIActive
Oticon 146979
FDA UDI
Class IIActive
Hhm 177209
FDA UDI
Class IIActive
Oticon 147176
FDA UDI
Class IIActive
Hhm 132320
FDA UDI
Class IIActive
Oticon 149519
FDA UDI
Class IIActive
Oticon 148990
FDA UDI
Class IIActive
Agxo 149606
FDA UDI
Class IIActive
Hhm 108883
FDA UDI
Class IIActive
Oticon 132381
FDA UDI
Class IIActive
Hhm 148979
FDA UDI
Class IIActive
Oticon 176637
FDA UDI
Class IIActive
Oticon 182597
FDA UDI
Class IIActive
Agxo 193309
FDA UDI
Class IIActive
EarQ 193374
FDA UDI
Class IIActive
Oticon 106-23-430-10
FDA UDI
Class IIActive
Agxo 150800
FDA UDI
Class IIActive
Oticon 135378
FDA UDI
Class IIActive
Oticon 131311
FDA UDI
Class IIActive
Agxo 118527
FDA UDI
Class IIActive
EarQ 201555
FDA UDI
Class IIActive
Oticon 140477
FDA UDI
Class IIActive
Agxo 193537
FDA UDI
Class IIActive
Agxo 133436
FDA UDI
Class IIActive
Oticon 129888
FDA UDI
Class IIActive
Agxo 133475
FDA UDI
Class IIActive
Hhm 119599
FDA UDI
Class IIActive
Oticon 113487
FDA UDI
Class IActive

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