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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 12 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 21176300
FDA UDI
Class IActive
GN ReSound 20591301
FDA UDI
Class IIUnknown
Beltone 20410800
FDA UDI
Class IIActive
GN ReSound 20257450
FDA UDI
Class IIUnknown
Beltone 21580605
FDA UDI
Class IIActive
GN Hearing 23088500
FDA UDI
Class IIActive
GN ReSound 20661501
FDA UDI
Class IIUnknown
GN ReSound 18342002
FDA UDI
Class IIUnknown
Beltone 20557451
FDA UDI
Class IIUnknown
GN ReSound 20331504
FDA UDI
Class IIUnknown
GN ReSound 19196708
FDA UDI
Class IIUnknown
GN Hearing 22502471
FDA UDI
Class IIActive
GN Hearing 22179600
FDA UDI
Class IIUnknown
Beltone TST6ITE-DW-UP
FDA UDI
Class IIUnknown
GN ReSound 20274200
FDA UDI
Class IUnknown
GN ReSound 20460108
FDA UDI
Class IIUnknown
GN ReSound 20262720
FDA UDI
Class IIUnknown
Beltone LND6MIH-S-UP
FDA UDI
Class IUnknown
GN ReSound 20155702
FDA UDI
Class IIUnknown
Beltone 22144170
FDA UDI
Class IIUnknown
GN Hearing 22015773
FDA UDI
Class IIActive
GN ReSound 18741010
FDA UDI
Class IIUnknown
GN ReSound 19542205
FDA UDI
Class IIUnknown
GN ReSound 21495804
FDA UDI
Class IIActive
GN Hearing 21879208
FDA UDI
Class IActive
GN ReSound 20647801
FDA UDI
Class IIActive
GN Hearing 22272573
FDA UDI
Class IIUnknown
Beltone 21226305
FDA UDI
Class IIActive
Beltone LND6ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound 20537505
FDA UDI
Class IIUnknown
GN Hearing 22147220
FDA UDI
Class IIActive
GN Hearing 22007520
FDA UDI
Class IIActive
GN ReSound LT7ITC-DW-UP
FDA UDI
Class IIUnknown
Beltone 19421101
FDA UDI
Class IIUnknown
GN ReSound 21495605
FDA UDI
Class IIActive
GN ReSound VO550-DW
FDA UDI
Class IIUnknown
GN ReSound 19196904
FDA UDI
Class IIUnknown
GN Hearing 22976372
FDA UDI
Class IIActive
GN ReSound 21506402
FDA UDI
Class IIActive
Beltone 19784300
FDA UDI
Class IUnknown
GN ReSound LS9ITE-W-UP
FDA UDI
Class IIUnknown
GN Hearing 19884602
FDA UDI
Class IIUnknown
GN ReSound 18289525
FDA UDI
Class IIUnknown
GN Hearing 22419400
FDA UDI
Class IIActive
GN ReSound 18288325
FDA UDI
Class IIUnknown
GN ReSound 18290220
FDA UDI
Class IIUnknown
GN Hearing 23545276
FDA UDI
Class IIActive
GN ReSound KE3CIC-LP
FDA UDI
Class IActive
GN Hearing 23814900
FDA UDI
Class IIActive
GN ReSound 21263850
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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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