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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 10 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 20977304
FDA UDI
Class IIUnknown
GN Hearing XD9CIC-LP
FDA UDI
Class IActive
GN ReSound 20709302
FDA UDI
Class IIUnknown
GN Hearing FP9ITC-LP
FDA UDI
Class IUnknown
GN ReSound 20559420
FDA UDI
Class IIUnknown
GN ReSound 20556908
FDA UDI
Class IIUnknown
GN ReSound 20307609
FDA UDI
Class IIUnknown
GN ReSound 19368250
FDA UDI
Class IIUnknown
Beltone 23304873
FDA UDI
Class IIActive
GN ReSound 23369278
FDA UDI
Class IIActive
Beltone AMZ6MIH-WT-HP
FDA UDI
Class IIActive
Beltone 21214320
FDA UDI
Class IIActive
GN Hearing 19403400
FDA UDI
Class IIUnknown
GN ReSound 20307325
FDA UDI
Class IIUnknown
GN Hearing 22015975
FDA UDI
Class IIActive
GN ReSound CL8MIH-W-MP
FDA UDI
Class IIUnknown
Beltone 22790271
FDA UDI
Class IIActive
GN Hearing 22945400
FDA UDI
Class IIActive
GN ReSound LT9MIH-W-MP
FDA UDI
Class IIUnknown
Beltone SER6ITC-DWC-HP
FDA UDI
Class IIActive
GN Hearing 23216372
FDA UDI
Class IIActive
GN ReSound 22176671
FDA UDI
Class IIActive
Beltone 21214502
FDA UDI
Class IIActive
GN Hearing 23545777
FDA UDI
Class IIActive
GN ReSound 21339670
FDA UDI
Class IIUnknown
GN ReSound 20333504
FDA UDI
Class IIUnknown
GN ReSound T9ITC-DW-UP
FDA UDI
Class IIUnknown
GN ReSound 19196705
FDA UDI
Class IIUnknown
GN ReSound 23347877
FDA UDI
Class IIActive
GN ReSound NX7CIC-LP
FDA UDI
Class IActive
Beltone 22082576
FDA UDI
Class IIUnknown
GN Hearing 22502870
FDA UDI
Class IIActive
Beltone AMZ6MIH-W-MP
FDA UDI
Class IIActive
GN ReSound 19698900
FDA UDI
Class IIUnknown
Beltone 19434800
FDA UDI
Class IUnknown
GN Hearing 22502871
FDA UDI
Class IIActive
GN ReSound RU9ITE-DWC-HP
FDA UDI
Class IIActive
GN ReSound L9MIH-W-MP
FDA UDI
Class IIUnknown
Beltone 22366777
FDA UDI
Class IIActive
GN Hearing 22170700
FDA UDI
Class IIUnknown
GN Hearing 21342877
FDA UDI
Class IIUnknown
GN ReSound FT8MIH-LP
FDA UDI
Class IUnknown
GN Hearing 22986171
FDA UDI
Class IIActive
GN ReSound 22081275
FDA UDI
Class IIUnknown
Beltone 22789875
FDA UDI
Class IIActive
GN Hearing 23558500
FDA UDI
Class IIActive
GN ReSound 20709020
FDA UDI
Class IIUnknown
GN Hearing 23766376
FDA UDI
Class IIActive
GN Hearing PK9CIC-HP
FDA UDI
Class IUnknown
GN Hearing 22232820
FDA UDI
Class IIActive

Related Companies

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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