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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 231 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 21732500
FDA UDI
Class IIUnknown
GN ReSound 22081772
FDA UDI
Class IIUnknown
GN ReSound 20333601
FDA UDI
Class IIUnknown
GN ReSound 21190409
FDA UDI
Class IIActive
Beltone TST17ITC-D-HP
FDA UDI
Class IUnknown
GN ReSound 21230802
FDA UDI
Class IIActive
GN ReSound 20332714
FDA UDI
Class IIUnknown
Beltone 20026509
FDA UDI
Class IIUnknown
GN ReSound 22176570
FDA UDI
Class IIActive
Beltone 20691102
FDA UDI
Class IIActive
GN ReSound 23347170
FDA UDI
Class IIActive
Beltone 19091604
FDA UDI
Class IIUnknown
GN ReSound 19209305
FDA UDI
Class IIUnknown
GN ReSound 22819000
FDA UDI
Class IIActive
Beltone 21580505
FDA UDI
Class IIActive
GN ReSound 19964409
FDA UDI
Class IIUnknown
GN ReSound KE3CIC-W-HP
FDA UDI
Class IIActive
GN ReSound 21230709
FDA UDI
Class IIActive
GN ReSound LT7CIC-W-HP
FDA UDI
Class IIUnknown
Beltone 23348275
FDA UDI
Class IIActive
GN ReSound RE4ITE-DW-MP
FDA UDI
Class IIActive
Beltone 20967876
FDA UDI
Class IIUnknown
GN ReSound 18289310
FDA UDI
Class IIUnknown
GN ReSound 19366800
FDA UDI
Class IUnknown
GN ReSound 21496602
FDA UDI
Class IIActive
GN ReSound 18741210
FDA UDI
Class IIUnknown
Beltone 19627604
FDA UDI
Class IIUnknown
Beltone AMZ6MIH-WT-MP
FDA UDI
Class IIActive
GN ReSound 23653200
FDA UDI
Class IIActive
GN ReSound 21213506
FDA UDI
Class IIActive
GN ReSound 20706004
FDA UDI
Class IIUnknown
Beltone 23387185
FDA UDI
Class IIActive
GN ReSound 20345120
FDA UDI
Class IIUnknown
GN ReSound 20072800
FDA UDI
Class IUnknown
Beltone 23347977
FDA UDI
Class IIActive
GN ReSound 22176472
FDA UDI
Class IIActive
GN ReSound RT7ITC-DWC-MP
FDA UDI
Class IIUnknown
GN ReSound 22168800
FDA UDI
Class IIUnknown
Beltone 21340573
FDA UDI
Class IIUnknown
Beltone AMZ6ITE-DW-MP
FDA UDI
Class IIActive
Beltone TST17ITC-DW-LP
FDA UDI
Class IIUnknown
Beltone TST9MIH-W-LP
FDA UDI
Class IIUnknown
Beltone 19628302
FDA UDI
Class IIUnknown
GN ReSound T5ITE-W-MP
FDA UDI
Class IIUnknown
GN ReSound 20591829
FDA UDI
Class IIUnknown
GN ReSound 21419311
FDA UDI
Class IIActive
Beltone 19368704
FDA UDI
Class IIUnknown
GN ReSound 20890700
FDA UDI
Class IIUnknown
GN ReSound 20734500
FDA UDI
Class IIUnknown
Beltone 20661000
FDA UDI
Class IIUnknown

Related Companies

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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