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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 21 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20591518
FDA UDI
Class IIUnknown
GN ReSound 20284200
FDA UDI
Class IIUnknown
GN Hearing 22975770
FDA UDI
Class IIActive
Beltone 21304374
FDA UDI
Class IIUnknown
GN ReSound 20457001
FDA UDI
Class IIUnknown
Beltone 23348172
FDA UDI
Class IIActive
Beltone 21264205
FDA UDI
Class IIActive
GN Hearing 18630200
FDA UDI
Class IIActive
GN ReSound LS7ITE-D-HP
FDA UDI
Class IUnknown
Beltone 22082475
FDA UDI
Class IIUnknown
GN ReSound 20591714
FDA UDI
Class IIUnknown
GN ReSound 20155710
FDA UDI
Class IIUnknown
GN ReSound 20070900
FDA UDI
Class IUnknown
GN ReSound 18741002
FDA UDI
Class IIUnknown
GN ReSound 19084102
FDA UDI
Class IIUnknown
GN ReSound 19209409
FDA UDI
Class IIUnknown
GN Hearing PK9IIC
FDA UDI
Class IUnknown
Beltone AY2ITE-DW-MP
FDA UDI
Class IIUnknown
GN ReSound 21213508
FDA UDI
Class IIActive
GN Hearing PK7ITC-D-HP
FDA UDI
Class IUnknown
GN Hearing 18627800
FDA UDI
Class IIActive
GN ReSound 20331505
FDA UDI
Class IIUnknown
Beltone LND6MIH-LP
FDA UDI
Class IUnknown
Beltone 20094808
FDA UDI
Class IIUnknown
Beltone 23348672
FDA UDI
Class IIActive
GN ReSound 22224400
FDA UDI
Class IIUnknown
GN ReSound 23347176
FDA UDI
Class IIActive
GN Hearing 23216271
FDA UDI
Class IIActive
GN Hearing 22019004
FDA UDI
Class IIUnknown
GN Hearing 20265401
FDA UDI
Class IIUnknown
GN ReSound 19190104
FDA UDI
Class IIUnknown
GN Hearing 18521600
FDA UDI
Class IActive
Beltone 20393701
FDA UDI
Class IIUnknown
GN ReSound 20914809
FDA UDI
Class IIUnknown
GN ReSound 21176600
FDA UDI
Class IActive
GN ReSound 20597114
FDA UDI
Class IIUnknown
GN ReSound 20284800
FDA UDI
Class IIUnknown
GN ReSound 22082077
FDA UDI
Class IIUnknown
GN Hearing 22015673
FDA UDI
Class IIActive
GN ReSound 20457418
FDA UDI
Class IIUnknown
Beltone 19705001
FDA UDI
Class IIUnknown
GN Hearing 22006120
FDA UDI
Class IIActive
GN ReSound CL8ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound EY2ITE-HP
FDA UDI
Class IUnknown
Beltone LND6ITE-W-HP
FDA UDI
Class IIUnknown
GN ReSound 19208705
FDA UDI
Class IIUnknown
Beltone 19807100
FDA UDI
Class IUnknown
GN Hearing XC2ITC-DW-HP
FDA UDI
Class IIActive
GN ReSound 20318600
FDA UDI
Class IIUnknown
GN Hearing 22928000
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

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