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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 32 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20472100
FDA UDI
Class IIUnknown
Beltone LND17ITE-DW-HP
FDA UDI
Class IIUnknown
GN Hearing 18581800
FDA UDI
Class IActive
GN Hearing 15477500
FDA UDI
Class IIActive
Beltone LND9ITC-W-HP
FDA UDI
Class IIUnknown
GN Hearing 20366804
FDA UDI
Class IIUnknown
GN ReSound 22445579
FDA UDI
Class IIActive
Beltone 22366676
FDA UDI
Class IIActive
Beltone 22173372
FDA UDI
Class IIActive
GN ReSound 19196906
FDA UDI
Class IIUnknown
GN ReSound 19962608
FDA UDI
Class IIUnknown
Beltone 19368709
FDA UDI
Class IIUnknown
GN ReSound 19368208
FDA UDI
Class IIUnknown
Beltone AMZ17ITE-DW-MP
FDA UDI
Class IIActive
Beltone LND17CIC-MP
FDA UDI
Class IUnknown
Beltone TST6ITE-D-MP
FDA UDI
Class IUnknown
GN ReSound LT9ITE-D-UP
FDA UDI
Class IUnknown
GN ReSound 20264504
FDA UDI
Class IIUnknown
GN Hearing 20273800
FDA UDI
Class IIUnknown
GN ReSound 18290314
FDA UDI
Class IIUnknown
GN Hearing 22502576
FDA UDI
Class IIActive
GN ReSound 20257414
FDA UDI
Class IIUnknown
GN Hearing 20291900
FDA UDI
Class IIActive
GN ReSound 19190025
FDA UDI
Class IIUnknown
GN ReSound 18805525
FDA UDI
Class IIUnknown
GN ReSound 20307652
FDA UDI
Class IIUnknown
GN ReSound 19361200
FDA UDI
Class IUnknown
Beltone 18266920
FDA UDI
Class IIUnknown
GN ReSound LT7ITE-W-HP
FDA UDI
Class IIUnknown
GN ReSound 19420918
FDA UDI
Class IIUnknown
GN Hearing 22986275
FDA UDI
Class IIActive
GN ReSound 22080778
FDA UDI
Class IIUnknown
GN Hearing 18582600
FDA UDI
Class IActive
Beltone AMZ9CIC-W-MP
FDA UDI
Class IIActive
GN Hearing 20619601
FDA UDI
Class IIUnknown
GN ReSound 20591418
FDA UDI
Class IIUnknown
GN ReSound 20345104
FDA UDI
Class IIUnknown
GN ReSound 20286800
FDA UDI
Class IIUnknown
GN Hearing 20268800
FDA UDI
Class IIUnknown
GN Hearing 20265105
FDA UDI
Class IIUnknown
Beltone TST6ITC-D-HP
FDA UDI
Class IUnknown
GN Hearing 21820100
FDA UDI
Class IIActive
GN ReSound LT9ITC-D-LP
FDA UDI
Class IUnknown
GN ReSound 19396910
FDA UDI
Class IIUnknown
Beltone 22789970
FDA UDI
Class IIActive
GN ReSound 21165052
FDA UDI
Class IIActive
GN ReSound 20449420
FDA UDI
Class IIUnknown
GN Hearing 23548089
FDA UDI
Class IIActive
GN ReSound 21193520
FDA UDI
Class IIActive
GN Hearing 20782710
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