Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 35 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20425400
FDA UDI
Class IIUnknown
GN ReSound 19706820
FDA UDI
Class IIUnknown
GN ReSound 23304674
FDA UDI
Class IIActive
GN ReSound 19190020
FDA UDI
Class IIUnknown
GN ReSound 23386588
FDA UDI
Class IIActive
GN Hearing XD7ITE-DWC-UP
FDA UDI
Class IIActive
Beltone 21283400
FDA UDI
Class IActive
Beltone AMZ17ITC-DW-MP
FDA UDI
Class IIActive
GN ReSound 20574213
FDA UDI
Class IIUnknown
GN Hearing 23545373
FDA UDI
Class IIActive
GN ReSound NX5ITE-DWC-HP
FDA UDI
Class IIActive
GN ReSound 20450200
FDA UDI
Class IIUnknown
GN Hearing 21265805
FDA UDI
Class IIUnknown
GN ReSound 21435520
FDA UDI
Class IIActive
GN ReSound 23386589
FDA UDI
Class IIActive
GN ReSound 20357701
FDA UDI
Class IIActive
GN ReSound 20701000
FDA UDI
Class IIUnknown
GN ReSound 17566120
FDA UDI
Class IUnknown
GN ReSound 18196101
FDA UDI
Class IIUnknown
GN Hearing EP2ITC-C-MP
FDA UDI
Class IIActive
Beltone 21147876
FDA UDI
Class IIUnknown
GN Hearing FP9ITC-HP
FDA UDI
Class IUnknown
GN ReSound 17841720
FDA UDI
Class IUnknown
GN ReSound 20075005
FDA UDI
Class IIUnknown
GN ReSound 20558611
FDA UDI
Class IIUnknown
GN ReSound 22485373
FDA UDI
Class IIActive
Beltone 21612500
FDA UDI
Class IIUnknown
GN Hearing 22985776
FDA UDI
Class IIActive
GN ReSound 20597106
FDA UDI
Class IIUnknown
GN ReSound 20537532
FDA UDI
Class IIUnknown
Beltone 18514002
FDA UDI
Class IIUnknown
Beltone 23348676
FDA UDI
Class IIActive
GN Hearing FP9ITC-D-HP
FDA UDI
Class IUnknown
GN ReSound 20558620
FDA UDI
Class IIUnknown
GN Hearing 23544873
FDA UDI
Class IIActive
GN ReSound 20536104
FDA UDI
Class IIUnknown
GN ReSound 20580304
FDA UDI
Class IIUnknown
GN ReSound LS7ITE-DW-HP
FDA UDI
Class IIUnknown
GN ReSound 19705804
FDA UDI
Class IIUnknown
GN ReSound 18741306
FDA UDI
Class IIUnknown
Beltone 22833874
FDA UDI
Class IIActive
Beltone 22486770
FDA UDI
Class IIActive
GN Hearing EP2ITC-LP
FDA UDI
Class IIActive
GN Hearing 22976070
FDA UDI
Class IIActive
Beltone 22082975
FDA UDI
Class IIUnknown
GN Hearing 22019404
FDA UDI
Class IIActive
GN ReSound 20591832
FDA UDI
Class IIUnknown
GN Hearing 22821472
FDA UDI
Class IIActive
GN ReSound 19706201
FDA UDI
Class IIUnknown
GN ReSound 19961602
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