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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 33 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22147876
FDA UDI
Class IIActive
GN Hearing PK9ITE-MP
FDA UDI
Class IUnknown
GN Hearing 19895600
FDA UDI
Class IIUnknown
GN ReSound LT9CIC-LP
FDA UDI
Class IUnknown
GN Hearing 23329404
FDA UDI
Class IIActive
GN ReSound L5MIH-W-LP
FDA UDI
Class IIUnknown
GN ReSound 20460620
FDA UDI
Class IIUnknown
Beltone 22834171
FDA UDI
Class IIActive
Beltone AMZ17MIH-WT-HP
FDA UDI
Class IIActive
Beltone 21164708
FDA UDI
Class IIActive
GN ReSound FT8MIH-HP
FDA UDI
Class IUnknown
Beltone 18267704
FDA UDI
Class IIUnknown
GN Hearing 19443200
FDA UDI
Class IIActive
GN ReSound 20536608
FDA UDI
Class IIUnknown
Beltone 18972608
FDA UDI
Class IIUnknown
GN ReSound LT9ITC-DW-HP
FDA UDI
Class IIUnknown
GN Hearing 22982674
FDA UDI
Class IIActive
GN Hearing 18501600
FDA UDI
Class IIActive
GN Hearing 23148900
FDA UDI
Class IIActive
GN ReSound 21539800
FDA UDI
Class IIUnknown
GN ReSound 23369270
FDA UDI
Class IIActive
GN Hearing 21885200
FDA UDI
Class IIUnknown
GN ReSound 18342406
FDA UDI
Class IIUnknown
GN Hearing 23216174
FDA UDI
Class IIActive
GN Hearing 20265301
FDA UDI
Class IIUnknown
GN ReSound 20262404
FDA UDI
Class IIUnknown
GN ReSound 20286400
FDA UDI
Class IIUnknown
GN Hearing XC3CIC-W-LP
FDA UDI
Class IIActive
Beltone AY2CIC-MP
FDA UDI
Class IUnknown
GN ReSound 19694400
FDA UDI
Class IIUnknown
GN Hearing 22503670
FDA UDI
Class IIActive
GN ReSound 19706608
FDA UDI
Class IIUnknown
GN ReSound LT7ITE-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 22822076
FDA UDI
Class IIActive
Beltone 21900700
FDA UDI
Class IIActive
GN ReSound LS5ITE-UP
FDA UDI
Class IUnknown
Beltone 19803100
FDA UDI
Class IUnknown
GN ReSound 18302401
FDA UDI
Class IIUnknown
GN ReSound 18290318
FDA UDI
Class IIUnknown
GN Hearing 20426501
FDA UDI
Class IIUnknown
GN Hearing 23370070
FDA UDI
Class IIActive
GN Hearing 22421100
FDA UDI
Class IIActive
Beltone 22082473
FDA UDI
Class IIUnknown
GN ReSound RT5ITC-DWC-LP
FDA UDI
Class IIUnknown
GN Hearing 18627900
FDA UDI
Class IIActive
GN ReSound 20460829
FDA UDI
Class IIUnknown
GN ReSound 20661409
FDA UDI
Class IIUnknown
Beltone 21581602
FDA UDI
Class IIActive
Beltone 19421105
FDA UDI
Class IIUnknown
Beltone 18267109
FDA UDI
Class IIUnknown

Related Companies

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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