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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 14 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22346200
FDA UDI
Class IIUnknown
Beltone RLY3ITC-DW-HP
FDA UDI
Class IIActive
Beltone 19784400
FDA UDI
Class IUnknown
GN ReSound 18805520
FDA UDI
Class IIUnknown
GN ReSound 18196125
FDA UDI
Class IIUnknown
GN ReSound 18741310
FDA UDI
Class IIUnknown
GN ReSound 22176676
FDA UDI
Class IIActive
GN Hearing 23760876
FDA UDI
Class IIActive
GN Hearing 23085000
FDA UDI
Class IIActive
GN ReSound 22835376
FDA UDI
Class IIActive
GN Hearing 22503770
FDA UDI
Class IIActive
GN ReSound 20251402
FDA UDI
Class IIUnknown
GN ReSound 18342425
FDA UDI
Class IIUnknown
Beltone 19212820
FDA UDI
Class IIUnknown
GN ReSound 22081278
FDA UDI
Class IIUnknown
GN Hearing 23670400
FDA UDI
Class IIActive
Beltone 21346902
FDA UDI
Class IIActive
GN Hearing 20780901
FDA UDI
Class IIUnknown
GN Hearing 22945100
FDA UDI
Class IIActive
Beltone 22083276
FDA UDI
Class IIUnknown
GN ReSound LS5MIH-W-MP
FDA UDI
Class IIUnknown
GN Hearing 22016377
FDA UDI
Class IIActive
GN ReSound 21213825
FDA UDI
Class IIActive
GN ReSound 19190010
FDA UDI
Class IIUnknown
Beltone 20344552
FDA UDI
Class IIUnknown
GN Hearing 22946500
FDA UDI
Class IIActive
GN Hearing 22822570
FDA UDI
Class IIActive
Beltone 21582602
FDA UDI
Class IIActive
GN Hearing 20273300
FDA UDI
Class IIUnknown
GN ReSound 20453405
FDA UDI
Class IIUnknown
GN ReSound 20094714
FDA UDI
Class IIUnknown
Beltone 19704804
FDA UDI
Class IIUnknown
GN ReSound 21497204
FDA UDI
Class IIActive
GN Hearing 20291300
FDA UDI
Class IIActive
GN ReSound 22082071
FDA UDI
Class IIUnknown
GN ReSound 22339571
FDA UDI
Class IIActive
Beltone 22173876
FDA UDI
Class IIActive
GN Hearing 23752500
FDA UDI
Class IIActive
GN ReSound 21435508
FDA UDI
Class IIActive
GN ReSound 20928609
FDA UDI
Class IIActive
GN Hearing 22452475
FDA UDI
Class IIActive
GN Hearing PK9MIH-S-HP
FDA UDI
Class IUnknown
Beltone AY3ITE-DW-MP
FDA UDI
Class IIUnknown
GN ReSound 20272400
FDA UDI
Class IUnknown
GN ReSound 19706801
FDA UDI
Class IIUnknown
GN Hearing 22147002
FDA UDI
Class IIUnknown
GN ReSound 19706904
FDA UDI
Class IIUnknown
GN Hearing PK9CIC-MP
FDA UDI
Class IUnknown
GN ReSound 18342014
FDA UDI
Class IIUnknown
GN ReSound 19208804
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