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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 7 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22900504
FDA UDI
Class IIActive
GN Hearing 22821776
FDA UDI
Class IIActive
Beltone 19212708
FDA UDI
Class IIUnknown
GN ReSound 18338514
FDA UDI
Class IIUnknown
Beltone 20648311
FDA UDI
Class IIActive
Beltone 18710100
FDA UDI
Class IUnknown
GN Hearing 23548088
FDA UDI
Class IIActive
GN ReSound 22789274
FDA UDI
Class IIActive
GN ReSound 20536408
FDA UDI
Class IIUnknown
Beltone 23369870
FDA UDI
Class IIActive
GN ReSound 19706710
FDA UDI
Class IIUnknown
GN ReSound 20085620
FDA UDI
Class IIUnknown
GN Hearing 23547572
FDA UDI
Class IIActive
GN Hearing FP9ITC-D-MP
FDA UDI
Class IUnknown
GN ReSound 21976100
FDA UDI
Class IIUnknown
Beltone 19703702
FDA UDI
Class IIUnknown
GN Hearing 23148300
FDA UDI
Class IIActive
GN ReSound 22081171
FDA UDI
Class IIUnknown
GN Hearing 23370174
FDA UDI
Class IIActive
Beltone 19212800
FDA UDI
Class IIUnknown
GN ReSound RT5ITE-DWC-UP
FDA UDI
Class IIActive
GN ReSound 19508602
FDA UDI
Class IIUnknown
GN ReSound LS7MIH-S-UP
FDA UDI
Class IUnknown
GN ReSound 20559209
FDA UDI
Class IIUnknown
GN ReSound 19196818
FDA UDI
Class IIUnknown
GN Hearing CH550-DW
FDA UDI
Class IIUnknown
GN ReSound 19397425
FDA UDI
Class IIUnknown
GN ReSound 23304673
FDA UDI
Class IIActive
GN Hearing 23722600
FDA UDI
Class IIActive
Beltone 21580805
FDA UDI
Class IIActive
Beltone 21312209
FDA UDI
Class IIActive
GN ReSound 17465120
FDA UDI
Class IUnknown
GN ReSound FT8MIH-W-HP
FDA UDI
Class IIUnknown
Beltone 22833876
FDA UDI
Class IIActive
GN Hearing EP2ITC-C-LP
FDA UDI
Class IIActive
Beltone 20156109
FDA UDI
Class IIUnknown
GN ReSound 21263750
FDA UDI
Class IIActive
GN Hearing 21304971
FDA UDI
Class IIUnknown
Beltone AMZ6MIH-WT-UP
FDA UDI
Class IIActive
GN Hearing 20782720
FDA UDI
Class IIUnknown
GN ReSound NX7ITC-DW-LP
FDA UDI
Class IIActive
Beltone 21304377
FDA UDI
Class IIUnknown
GN ReSound RE9ITE-DWT-UP
FDA UDI
Class IIActive
GN ReSound 20371609
FDA UDI
Class IIUnknown
GN ReSound 18958001
FDA UDI
Class IIUnknown
GN Hearing 23839700
FDA UDI
Class IIActive
GN ReSound 18288101
FDA UDI
Class IIUnknown
GN Hearing 23547075
FDA UDI
Class IIActive
GN ReSound 21193518
FDA UDI
Class IIActive
GN Hearing 21945591
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

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Authorities

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FDA Establishments (1)

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

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