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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 19 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 18290309
FDA UDI
Class IIUnknown
GN Hearing 22277520
FDA UDI
Class IIActive
GN Hearing 15476600
FDA UDI
Class IIActive
GN ReSound CL8ITC-HP
FDA UDI
Class IUnknown
Beltone 19703808
FDA UDI
Class IIUnknown
Beltone 23348276
FDA UDI
Class IIActive
GN ReSound 22835372
FDA UDI
Class IIActive
GN ReSound RE4ITE-DW-UP
FDA UDI
Class IIActive
GN ReSound 20591705
FDA UDI
Class IIUnknown
GN ReSound 20537214
FDA UDI
Class IIUnknown
GN ReSound 19078850
FDA UDI
Class IIUnknown
GN ReSound 20094705
FDA UDI
Class IIUnknown
GN Hearing 23685870
FDA UDI
Class IIActive
GN ReSound 23176073
FDA UDI
Class IIActive
Beltone 22173277
FDA UDI
Class IIActive
Beltone SER17ITC-DW-HP
FDA UDI
Class IIActive
Beltone 20551610
FDA UDI
Class IIUnknown
GN ReSound 23347678
FDA UDI
Class IIActive
Beltone PSE645-DPW
FDA UDI
Class IIUnknown
GN ReSound 19185204
FDA UDI
Class IActive
GN Hearing 23685770
FDA UDI
Class IIActive
GN Hearing 21878801
FDA UDI
Class IActive
GN ReSound 20537325
FDA UDI
Class IIUnknown
GN Hearing 23544575
FDA UDI
Class IIActive
Beltone AY3CIC-UP
FDA UDI
Class IUnknown
GN ReSound VE350-DP
FDA UDI
Class IUnknown
GN Hearing 22355500
FDA UDI
Class IIActive
GN ReSound 22080770
FDA UDI
Class IIUnknown
GN ReSound 23119600
FDA UDI
Class IIActive
Beltone 22173370
FDA UDI
Class IIActive
GN Hearing 20619904
FDA UDI
Class IIUnknown
GN ReSound 20307309
FDA UDI
Class IIUnknown
GN Hearing 23086300
FDA UDI
Class IIActive
GN Hearing 23216677
FDA UDI
Class IIActive
GN Hearing 20967676
FDA UDI
Class IIUnknown
Beltone 21304370
FDA UDI
Class IIUnknown
GN ReSound T9ITE-DW-HP
FDA UDI
Class IIUnknown
GN Hearing 21249425
FDA UDI
Class IIUnknown
Beltone TST9ITC-LP
FDA UDI
Class IUnknown
Beltone 21539370
FDA UDI
Class IIUnknown
Beltone 23348674
FDA UDI
Class IIActive
GN Hearing 23129000
FDA UDI
Class IIActive
Beltone 18267909
FDA UDI
Class IIUnknown
GN ReSound EY3ITC-HP
FDA UDI
Class IUnknown
Beltone 15682000
FDA UDI
Class IIUnknown
GN Hearing 23547987
FDA UDI
Class IIActive
GN ReSound 23369377
FDA UDI
Class IIActive
GN ReSound 21211651
FDA UDI
Class IIActive
GN ReSound 21211610
FDA UDI
Class IIActive
GN ReSound 21279400
FDA UDI
Class IActive

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