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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 46 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 21496120
FDA UDI
Class IIActive
GN Hearing 22502876
FDA UDI
Class IIActive
Beltone 21231202
FDA UDI
Class IIActive
GN ReSound LS5ITC-W-LP
FDA UDI
Class IIUnknown
GN ReSound T7ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound 20460705
FDA UDI
Class IIUnknown
GN Hearing 18655700
FDA UDI
Class IIActive
GN ReSound 20591425
FDA UDI
Class IIUnknown
GN Hearing 22822772
FDA UDI
Class IIActive
GN Hearing 21384500
FDA UDI
Class IActive
GN ReSound 20647920
FDA UDI
Class IIActive
GN Hearing 22270770
FDA UDI
Class IIUnknown
Beltone 21226409
FDA UDI
Class IIActive
GN ReSound 20457320
FDA UDI
Class IIUnknown
GN Hearing PKX9CIC-LP
FDA UDI
Class IUnknown
Beltone 20393902
FDA UDI
Class IIUnknown
GN Hearing 18628700
FDA UDI
Class IIActive
Beltone 20648104
FDA UDI
Class IIActive
GN Hearing 18501400
FDA UDI
Class IIActive
Beltone 19703308
FDA UDI
Class IIUnknown
GN ReSound 22143470
FDA UDI
Class IIUnknown
Beltone 21580402
FDA UDI
Class IIActive
Beltone 20735009
FDA UDI
Class IIActive
GN ReSound 19368404
FDA UDI
Class IIUnknown
Beltone 22789873
FDA UDI
Class IIActive
GN Hearing FP7ITC-UP
FDA UDI
Class IUnknown
GN ReSound T9ITE-DW-MP
FDA UDI
Class IIUnknown
GN ReSound 18338420
FDA UDI
Class IIUnknown
GN ReSound 21316615
FDA UDI
Class IIUnknown
GN ReSound 23347270
FDA UDI
Class IIActive
GN ReSound NX9CIC-HP
FDA UDI
Class IActive
Beltone 22833670
FDA UDI
Class IIActive
GN Hearing 22235800
FDA UDI
Class IIUnknown
GN Hearing XF5ITE-DWC-MP
FDA UDI
Class IIActive
GN Hearing 22944070
FDA UDI
Class IIActive
GN ReSound RU7ITC-DWC-LP
FDA UDI
Class IIActive
GN Hearing 22271074
FDA UDI
Class IIUnknown
GN ReSound 20313729
FDA UDI
Class IIUnknown
GN ReSound PZ8CIC-W-LP
FDA UDI
Class IIActive
GN Hearing 23545170
FDA UDI
Class IIActive
GN Hearing 23372100
FDA UDI
Class IIActive
GN ReSound LS5MIH-HP
FDA UDI
Class IUnknown
GN ReSound 21213501
FDA UDI
Class IIActive
GN ReSound 22061400
FDA UDI
Class IIUnknown
GN ReSound LS9MIH-MP
FDA UDI
Class IUnknown
GN Hearing 20040500
FDA UDI
Class IIActive
GN Hearing 23546571
FDA UDI
Class IIActive
Beltone 22790273
FDA UDI
Class IIActive
GN ReSound 21496004
FDA UDI
Class IIActive
Beltone 23387187
FDA UDI
Class IIActive

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