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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 1 of 232
DeviceModel / ReferenceRegistriesClassStatus
Beltone 22789976
FDA UDI
Class IIActive
Beltone 21211809
FDA UDI
Class IIActive
GN Hearing 21306700
FDA UDI
Class IActive
Beltone 21224202
FDA UDI
Class IIActive
GN Hearing CH950-DW
FDA UDI
Class IIUnknown
Beltone PSE1735-DPW
FDA UDI
Class IIUnknown
GN Hearing 22976376
FDA UDI
Class IIActive
Beltone PSE635-W
FDA UDI
Class IIUnknown
GN ReSound 18288218
FDA UDI
Class IIUnknown
Beltone 22174075
FDA UDI
Class IIActive
Beltone 21192004
FDA UDI
Class IIActive
GN ReSound 20453304
FDA UDI
Class IIUnknown
GN ReSound 19705850
FDA UDI
Class IIUnknown
GN ReSound 20710302
FDA UDI
Class IIUnknown
GN Hearing 22008076
FDA UDI
Class IIUnknown
GN Hearing 22850475
FDA UDI
Class IIActive
Beltone TST9ITE-W-HP
FDA UDI
Class IIUnknown
GN ReSound 19091509
FDA UDI
Class IIUnknown
GN Hearing 22982771
FDA UDI
Class IIActive
Beltone 19705011
FDA UDI
Class IIUnknown
GN ReSound 20257520
FDA UDI
Class IIUnknown
GN Hearing 22007320
FDA UDI
Class IIActive
GN ReSound 20331804
FDA UDI
Class IIUnknown
Beltone 19963000
FDA UDI
Class IIUnknown
GN Hearing 22502872
FDA UDI
Class IIActive
Beltone 20393911
FDA UDI
Class IIUnknown
GN ReSound 18290325
FDA UDI
Class IIUnknown
GN ReSound 18288109
FDA UDI
Class IIUnknown
GN ReSound 19191409
FDA UDI
Class IIUnknown
GN ReSound 22081173
FDA UDI
Class IIUnknown
GN ReSound LS9MIH-W-LP
FDA UDI
Class IIUnknown
GN Hearing 22179900
FDA UDI
Class IIUnknown
GN ReSound 20647925
FDA UDI
Class IIActive
GN ReSound 20536711
FDA UDI
Class IIUnknown
GN ReSound LT7ITC-W-MP
FDA UDI
Class IIUnknown
Beltone LND6ITC-W-LP
FDA UDI
Class IIUnknown
GN Hearing 23546471
FDA UDI
Class IIActive
Beltone IMP17CIC-MP
FDA UDI
Class IActive
GN ReSound 21506808
FDA UDI
Class IIActive
GN ReSound 21496302
FDA UDI
Class IIActive
GN Hearing 21002620
FDA UDI
Class IIUnknown
GN Hearing PKX9ITE-W-MP
FDA UDI
Class IIUnknown
GN Hearing FP9ITC-D-UP
FDA UDI
Class IUnknown
Beltone 19703220
FDA UDI
Class IIUnknown
Beltone 19421004
FDA UDI
Class IIUnknown
GN ReSound 21197304
FDA UDI
Class IIActive
GN Hearing 21002920
FDA UDI
Class IIUnknown
GN ReSound 22834876
FDA UDI
Class IIActive
GN ReSound 21303974
FDA UDI
Class IIUnknown
GN Hearing PKX9ITC-D-UP
FDA UDI
Class IUnknown

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