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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 9 of 232
DeviceModel / ReferenceRegistriesClassStatus
Beltone 22082378
FDA UDI
Class IIUnknown
Beltone 18267900
FDA UDI
Class IIUnknown
GN ReSound 21193908
FDA UDI
Class IIActive
GN ReSound 19706606
FDA UDI
Class IIUnknown
GN ReSound 21165025
FDA UDI
Class IIActive
GN ReSound T5MIH-W-MP
FDA UDI
Class IIUnknown
GN ReSound 20155950
FDA UDI
Class IIUnknown
GN ReSound 20457525
FDA UDI
Class IIUnknown
GN ReSound 19706108
FDA UDI
Class IIUnknown
GN ReSound 22834977
FDA UDI
Class IIActive
GN ReSound 23304470
FDA UDI
Class IIActive
Beltone 22173873
FDA UDI
Class IIActive
GN ReSound 23386485
FDA UDI
Class IIActive
GN ReSound 21213805
FDA UDI
Class IIActive
Beltone 23348277
FDA UDI
Class IIActive
Beltone 21193611
FDA UDI
Class IIActive
GN Hearing 19403900
FDA UDI
Class IIUnknown
GN ReSound 20661504
FDA UDI
Class IIUnknown
GN ReSound T5ITC-DW-HP
FDA UDI
Class IIUnknown
GN Hearing 22448800
FDA UDI
Class IIActive
GN Hearing 21655500
FDA UDI
Class IIActive
GN Hearing FL7ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound 23098470
FDA UDI
Class IIActive
GN Hearing 23217270
FDA UDI
Class IIActive
GN ReSound 22222400
FDA UDI
Class IIUnknown
Beltone 22226300
FDA UDI
Class IIUnknown
GN ReSound Y2ITC-W-LP
FDA UDI
Class IIUnknown
GN ReSound 21506502
FDA UDI
Class IIActive
GN ReSound 21435705
FDA UDI
Class IIActive
GN ReSound 20591310
FDA UDI
Class IIUnknown
GN ReSound 20536911
FDA UDI
Class IIUnknown
Beltone 19785500
FDA UDI
Class IUnknown
GN Hearing 20294100
FDA UDI
Class IIActive
GN ReSound 19707052
FDA UDI
Class IIUnknown
Beltone 20358902
FDA UDI
Class IIUnknown
GN ReSound 21211604
FDA UDI
Class IIActive
GN Hearing 19884502
FDA UDI
Class IIUnknown
GN Hearing 21972900
FDA UDI
Class IIActive
Beltone 21539374
FDA UDI
Class IIUnknown
Beltone AMZ17CIC-W-MP
FDA UDI
Class IIActive
GN Hearing 20268900
FDA UDI
Class IIUnknown
Beltone 17862108
FDA UDI
Class IIUnknown
GN ReSound 20331905
FDA UDI
Class IIUnknown
GN ReSound 19397410
FDA UDI
Class IIUnknown
GN ReSound 22338171
FDA UDI
Class IIActive
Beltone 22082875
FDA UDI
Class IIUnknown
GN Hearing 22503572
FDA UDI
Class IIActive
Beltone 22833973
FDA UDI
Class IIActive
GN ReSound T9ITC-W-UP
FDA UDI
Class IIUnknown
Beltone LND9MIH-UP
FDA UDI
Class IUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

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