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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 3 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 18288306
FDA UDI
Class IIUnknown
GN ReSound FT8IIC-LP
FDA UDI
Class IUnknown
GN ReSound 21497304
FDA UDI
Class IIActive
GN Hearing 22821870
FDA UDI
Class IIActive
GN ReSound 19287625
FDA UDI
Class IIUnknown
GN ReSound 22835175
FDA UDI
Class IIActive
GN ReSound 20558602
FDA UDI
Class IIUnknown
Beltone 20552610
FDA UDI
Class IIUnknown
GN ReSound 18308306
FDA UDI
Class IIUnknown
GN Hearing 22007971
FDA UDI
Class IIUnknown
GN ReSound 21184829
FDA UDI
Class IIActive
GN ReSound 20371605
FDA UDI
Class IIUnknown
Beltone PSE635-PW
FDA UDI
Class IIUnknown
GN Hearing 22822376
FDA UDI
Class IIActive
GN ReSound 23176075
FDA UDI
Class IIActive
GN ReSound 22143876
FDA UDI
Class IIUnknown
GN ReSound 20460308
FDA UDI
Class IIUnknown
GN Hearing XC3CIC-W-HP
FDA UDI
Class IIActive
GN Hearing XF9ITC-DWC-HP
FDA UDI
Class IIActive
Beltone 22834572
FDA UDI
Class IIActive
GN ReSound L7MIH-W-HP
FDA UDI
Class IIUnknown
GN Hearing 19462900
FDA UDI
Class IIUnknown
GN Hearing 21599914
FDA UDI
Class IIUnknown
Beltone OR235-P
FDA UDI
Class IUnknown
Beltone 19091611
FDA UDI
Class IIUnknown
GN Hearing 22007772
FDA UDI
Class IIUnknown
GN ReSound 20457208
FDA UDI
Class IIUnknown
GN ReSound 20708901
FDA UDI
Class IIUnknown
GN ReSound VE330-P
FDA UDI
Class IUnknown
Beltone 21224204
FDA UDI
Class IIActive
GN Hearing 20780718
FDA UDI
Class IIUnknown
GN ReSound 22834871
FDA UDI
Class IIActive
GN ReSound 22620400
FDA UDI
Class IIActive
GN ReSound 22835577
FDA UDI
Class IIActive
Beltone AMZ6CIC-W-HP
FDA UDI
Class IIActive
GN Hearing 22007008
FDA UDI
Class IIActive
GN ReSound LT5ITE-W-MP
FDA UDI
Class IIUnknown
GN ReSound NX7ITC-DWC-UP
FDA UDI
Class IIActive
Beltone 22356400
FDA UDI
Class IIActive
GN Hearing 21266004
FDA UDI
Class IIUnknown
GN ReSound 20345105
FDA UDI
Class IIUnknown
Beltone 19212702
FDA UDI
Class IIUnknown
Beltone 19376500
FDA UDI
Class IUnknown
GN ReSound 20537010
FDA UDI
Class IIUnknown
GN Hearing 22943971
FDA UDI
Class IIActive
Beltone LND9CIC-LP
FDA UDI
Class IUnknown
GN ReSound L9ITE-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 22019920
FDA UDI
Class IIActive
Beltone 21582409
FDA UDI
Class IIActive
GN Hearing 23546286
FDA UDI
Class IIActive

Related Companies

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Notified Bodies

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • GN Hearing A/S BALLERUP Hovedstaden · DK FEI 3005650109