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Gn Hearing A/S

US

Last updated May 24, 2026

What Gn Hearing A/S makes

The company manufactures air-conduction hearing aids in various styles, including receiver-in-canal, behind-the-ear, canal, and in-the-ear designs, as well as custom-made earmoulds and acoustic tubes. Their portfolio also includes noninvasive battery chargers for hearing devices and audiometric/hearing device software for diagnostic and testing purposes.

These devices are regulated under the FDA’s UDI system, with classifications ranging from Class I to Class II. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, reflecting their compliance with U.S. regulatory requirements.

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 Gn Hearing A/S manufacture?

Gn Hearing A/S specializes in air-conduction hearing aids, which come in multiple styles such as receiver-in-canal, behind-the-ear, canal, and in-the-ear designs. Their portfolio also includes custom-made earmoulds, acoustic tubes for hearing aids, noninvasive battery chargers for hearing devices, and audiometric/hearing device software used for diagnostics and testing. These products address hearing loss and related audiometric needs.

Where is Gn Hearing A/S based, and how does that affect its regulatory standing?

Gn Hearing A/S is based in the United States, which means its devices fall under U.S. regulatory oversight. Since the company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, they comply with U.S. requirements for medical device registration and classification. The FDA categorizes these devices as either Class I or Class II, depending on their risk level and intended use.

Which regulatory registries list Gn Hearing A/S’s devices?

Gn Hearing A/S’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures transparency and traceability of medical devices under U.S. regulatory standards, allowing healthcare providers, regulators, and patients to verify product details, classifications, and compliance status. Listing in this database reflects adherence to FDA requirements for device identification and tracking.

How are Gn Hearing A/S’s hearing aids classified under U.S. regulations?

Gn Hearing A/S’s hearing aids are classified as either Class I or Class II devices under FDA regulations. The classification depends on factors like the device’s risk level, intended use, and potential impact on patient safety. For example, simpler hearing aids with low risk may fall under Class I, while more complex or higher-risk devices (such as those with advanced software or custom components) may be classified as Class II. This classification determines the regulatory controls and reporting requirements applied to the device.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
gnresound.com
LinkedIn
—
Facebook
—
Phone
+1-888-735-4327
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
306179227

Catalogue (11594)

Page 22 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22975974
FDA UDI
Class IIActive
Beltone AMZ17ITC-DW-HP
FDA UDI
Class IIActive
GN Hearing 20294200
FDA UDI
Class IIActive
Beltone 19368820
FDA UDI
Class IIUnknown
Beltone 23369572
FDA UDI
Class IIActive
GN Hearing 22976170
FDA UDI
Class IIActive
GN ReSound CL8CIC-MP
FDA UDI
Class IUnknown
GN Hearing 19709600
FDA UDI
Class IIActive
GN ReSound 21506902
FDA UDI
Class IIActive
GN ReSound 20537208
FDA UDI
Class IIUnknown
GN Hearing 20265705
FDA UDI
Class IIUnknown
Beltone 22173471
FDA UDI
Class IIActive
GN Hearing 23117700
FDA UDI
Class IIActive
GN Hearing XB7ITE-DWC-MP
FDA UDI
Class IIUnknown
GN ReSound 18338302
FDA UDI
Class IIUnknown
Beltone 22790376
FDA UDI
Class IIActive
GN Hearing 23546470
FDA UDI
Class IIActive
Beltone 19368611
FDA UDI
Class IIUnknown
GN ReSound 20262902
FDA UDI
Class IIUnknown
GN ReSound 20094620
FDA UDI
Class IIUnknown
GN ReSound 20269900
FDA UDI
Class IUnknown
Beltone 22057600
FDA UDI
Class IIUnknown
GN ReSound 21969210
FDA UDI
Class IIUnknown
GN ReSound 19209406
FDA UDI
Class IIUnknown
GN ReSound RE9ITE-DW-UP
FDA UDI
Class IIActive
GN ReSound 20537402
FDA UDI
Class IIUnknown
GN ReSound 23653100
FDA UDI
Class IIActive
GN ReSound EY3ITE-DW-UP
FDA UDI
Class IIUnknown
Beltone 19421002
FDA UDI
Class IIUnknown
GN Hearing 20780814
FDA UDI
Class IIUnknown
GN ReSound 21213408
FDA UDI
Class IIActive
Beltone 22173772
FDA UDI
Class IIActive
GN ReSound 21278200
FDA UDI
Class IActive
GN Hearing 22227900
FDA UDI
Class IIActive
GN Hearing 22268402
FDA UDI
Class IIActive
GN ReSound 20928602
FDA UDI
Class IIActive
GN Hearing FP7ITC-D-UP
FDA UDI
Class IUnknown
GN ReSound T9ITC-W-HP
FDA UDI
Class IIUnknown
GN ReSound 21339774
FDA UDI
Class IIUnknown
Beltone LND9MIH-S-HP
FDA UDI
Class IUnknown
GN Hearing 22067490
FDA UDI
Class IIActive
GN ReSound 20648004
FDA UDI
Class IIActive
GN ReSound 20261904
FDA UDI
Class IIUnknown
GN ReSound 19706209
FDA UDI
Class IIUnknown
GN ReSound 22851300
FDA UDI
Class IIActive
Beltone RLY3ITE-DW-HP
FDA UDI
Class IIActive
GN Hearing 23116800
FDA UDI
Class IIActive
GN Hearing 22821477
FDA UDI
Class IIActive
GN Hearing XB5ITE-DWC-HP
FDA UDI
Class IIUnknown
GN ReSound L7ITC-W-HP
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

Not available yet.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • GN Hearing A/S BALLERUP Hovedstaden · DK FEI 3005650109