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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 27 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound RE7ITC-DWT-HP
FDA UDI
Class IIActive
GN ReSound 21213820
FDA UDI
Class IIActive
GN Hearing 22161801
FDA UDI
Class IIActive
GN Hearing 21643600
FDA UDI
Class IActive
GN ReSound 20460810
FDA UDI
Class IIUnknown
Beltone 18710504
FDA UDI
Class IIUnknown
GN ReSound 19196610
FDA UDI
Class IIUnknown
GN ReSound RE7ITE-DWT-HP
FDA UDI
Class IIActive
Beltone 18268500
FDA UDI
Class IIUnknown
GN Hearing 23546876
FDA UDI
Class IIActive
GN ReSound 19397420
FDA UDI
Class IIUnknown
GN ReSound 22081577
FDA UDI
Class IIUnknown
GN ReSound 22834970
FDA UDI
Class IIActive
GN ReSound VE230
FDA UDI
Class IUnknown
GN ReSound 23347779
FDA UDI
Class IIActive
GN ReSound T7ITC-DW-MP
FDA UDI
Class IIUnknown
GN ReSound LS7ITC-D-UP
FDA UDI
Class IUnknown
GN ReSound 20734400
FDA UDI
Class IIUnknown
GN ReSound 20585402
FDA UDI
Class IIUnknown
GN ReSound 19185120
FDA UDI
Class IUnknown
GN ReSound 19190209
FDA UDI
Class IIUnknown
GN Hearing 22502976
FDA UDI
Class IIActive
GN Hearing 21384800
FDA UDI
Class IActive
Beltone 21231302
FDA UDI
Class IIActive
GN ReSound 20345152
FDA UDI
Class IIUnknown
GN ReSound 20357806
FDA UDI
Class IIUnknown
GN ReSound 22080874
FDA UDI
Class IIUnknown
Beltone LND9ITE-W-MP
FDA UDI
Class IIUnknown
Beltone 17863701
FDA UDI
Class IIUnknown
GN ReSound 21509200
FDA UDI
Class IIActive
GN ReSound 21196432
FDA UDI
Class IIActive
GN Hearing 20781008
FDA UDI
Class IIUnknown
Beltone 23304879
FDA UDI
Class IIActive
GN ReSound 18196104
FDA UDI
Class IIUnknown
Beltone 21190100
FDA UDI
Class IActive
GN ReSound 21139300
FDA UDI
Class IIUnknown
GN Hearing 23216577
FDA UDI
Class IIActive
GN Hearing 23118500
FDA UDI
Class IIActive
GN ReSound 20928601
FDA UDI
Class IIActive
GN Hearing 21641700
FDA UDI
Class IActive
GN ReSound 20289900
FDA UDI
Class IIUnknown
GN ReSound 18290306
FDA UDI
Class IIUnknown
GN Hearing 22007002
FDA UDI
Class IIActive
GN ReSound 19196702
FDA UDI
Class IIUnknown
GN Hearing 23770600
FDA UDI
Class IIActive
GN Hearing 21305175
FDA UDI
Class IIUnknown
GN ReSound PZ8ITE-DW-UP
FDA UDI
Class IIActive
GN ReSound 21213425
FDA UDI
Class IIActive
GN ReSound 19368501
FDA UDI
Class IIUnknown
GN ReSound RT9CIC-MP
FDA UDI
Class IUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

Not available yet.

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