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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 37 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 19196514
FDA UDI
Class IIUnknown
GN ReSound 22176677
FDA UDI
Class IIActive
GN Hearing 22271474
FDA UDI
Class IIUnknown
GN ReSound 22175771
FDA UDI
Class IIActive
GN ReSound 20457104
FDA UDI
Class IIUnknown
GN ReSound 18573934
FDA UDI
Class IIUnknown
GN Hearing 22015877
FDA UDI
Class IIActive
GN ReSound LT9ITE-HP
FDA UDI
Class IUnknown
Beltone 19368904
FDA UDI
Class IIUnknown
GN ReSound 22341674
FDA UDI
Class IIActive
GN ReSound 20661608
FDA UDI
Class IIUnknown
GN ReSound 20556825
FDA UDI
Class IIUnknown
GN ReSound T5ITC-W-MP
FDA UDI
Class IIUnknown
GN ReSound NX9ITE-DWC-HP
FDA UDI
Class IIActive
GN Hearing 22275270
FDA UDI
Class IIUnknown
GN Hearing 20367204
FDA UDI
Class IIUnknown
GN ReSound 19706501
FDA UDI
Class IIUnknown
Beltone 19627704
FDA UDI
Class IIUnknown
GN Hearing XF9ITE-DWC-MP
FDA UDI
Class IIActive
GN ReSound NX7ITE-DWC-UP
FDA UDI
Class IIActive
GN Hearing 21342976
FDA UDI
Class IIUnknown
GN ReSound 20345110
FDA UDI
Class IIUnknown
GN ReSound 20072600
FDA UDI
Class IUnknown
GN Hearing 22268503
FDA UDI
Class IIActive
GN Hearing 21878802
FDA UDI
Class IActive
GN Hearing FP7ITC-LP
FDA UDI
Class IUnknown
GN ReSound 20403402
FDA UDI
Class IIUnknown
GN ReSound 20537329
FDA UDI
Class IIUnknown
GN ReSound 21211552
FDA UDI
Class IIActive
GN ReSound 20710204
FDA UDI
Class IIUnknown
Beltone 21582620
FDA UDI
Class IIActive
GN Hearing 22006804
FDA UDI
Class IIActive
Beltone 19368602
FDA UDI
Class IIUnknown
GN Hearing 18580600
FDA UDI
Class IActive
GN ReSound 20413910
FDA UDI
Class IIActive
GN ReSound 20591325
FDA UDI
Class IIUnknown
GN Hearing 20424200
FDA UDI
Class IIUnknown
GN Hearing 22016375
FDA UDI
Class IIActive
GN Hearing 21631700
FDA UDI
Class IIUnknown
Beltone PSE645-DW
FDA UDI
Class IIUnknown
Beltone 19785300
FDA UDI
Class IUnknown
GN ReSound 21398000
FDA UDI
Class IIActive
GN Hearing 22982676
FDA UDI
Class IIActive
GN ReSound LT9ITC-DW-MP
FDA UDI
Class IIUnknown
GN ReSound LT5ITC-DW-UP
FDA UDI
Class IIUnknown
Beltone 19397202
FDA UDI
Class IIUnknown
Beltone 23387488
FDA UDI
Class IIActive
GN ReSound 20331720
FDA UDI
Class IIUnknown
GN ReSound 18288320
FDA UDI
Class IIUnknown
GN ReSound 19542408
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

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