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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 54 of 232
DeviceModel / ReferenceRegistriesClassStatus
Beltone 20557509
FDA UDI
Class IIUnknown
GN Hearing XB7ITE-DWC-UP
FDA UDI
Class IIUnknown
GN ReSound 18289510
FDA UDI
Class IIUnknown
GN Hearing 21644000
FDA UDI
Class IActive
GN ReSound 20460209
FDA UDI
Class IIUnknown
GN ReSound 20155705
FDA UDI
Class IIUnknown
Beltone PSE1735-DW
FDA UDI
Class IIUnknown
GN ReSound 19706925
FDA UDI
Class IIUnknown
GN ReSound 18654202
FDA UDI
Class IIUnknown
Beltone 18267901
FDA UDI
Class IIUnknown
GN Hearing 22148474
FDA UDI
Class IIActive
Beltone 18267420
FDA UDI
Class IIUnknown
GN ReSound KE4CIC-W-HP
FDA UDI
Class IIActive
Beltone 22833570
FDA UDI
Class IIActive
GN Hearing 20294600
FDA UDI
Class IIActive
GN ReSound 21230850
FDA UDI
Class IIActive
GN Hearing 20780732
FDA UDI
Class IIUnknown
GN Hearing 22985975
FDA UDI
Class IIActive
Beltone 21790400
FDA UDI
Class IIActive
GN Hearing 20426420
FDA UDI
Class IIUnknown
GN ReSound 19707008
FDA UDI
Class IIUnknown
GN ReSound 18289506
FDA UDI
Class IIUnknown
GN Hearing CH530-MUW
FDA UDI
Class IIUnknown
GN Hearing 22008476
FDA UDI
Class IIUnknown
GN Hearing PK9MIH-S-UP
FDA UDI
Class IUnknown
GN Hearing 18839300
FDA UDI
Class IIActive
Beltone OR245
FDA UDI
Class IUnknown
GN Hearing 21597700
FDA UDI
Class IIUnknown
GN ReSound 19964318
FDA UDI
Class IIUnknown
Beltone AY3ITE-MP
FDA UDI
Class IUnknown
Beltone 20094811
FDA UDI
Class IIUnknown
Beltone 18268308
FDA UDI
Class IIUnknown
GN ReSound 20257408
FDA UDI
Class IIUnknown
GN Hearing XF9ITC-DW-MP
FDA UDI
Class IIActive
GN Hearing XF7ITE-DWC-MP
FDA UDI
Class IIActive
GN ReSound RU9ITC-DWC-LP
FDA UDI
Class IIActive
Beltone 22082574
FDA UDI
Class IIUnknown
GN ReSound 22080772
FDA UDI
Class IIUnknown
Beltone 21178200
FDA UDI
Class IActive
Beltone 20648105
FDA UDI
Class IIActive
GN ReSound 20262401
FDA UDI
Class IIUnknown
GN ReSound LS7MIH-MP
FDA UDI
Class IUnknown
GN ReSound 20093609
FDA UDI
Class IIUnknown
GN ReSound 19191309
FDA UDI
Class IIUnknown
GN ReSound KE2ITE-DW-UP
FDA UDI
Class IIActive
GN ReSound 21497120
FDA UDI
Class IIActive
GN ReSound VO950-PW
FDA UDI
Class IIUnknown
Beltone 18020800
FDA UDI
Class IUnknown
GN ReSound 19360800
FDA UDI
Class IUnknown
GN ReSound 18308718
FDA UDI
Class IIUnknown

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