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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 17 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20536204
FDA UDI
Class IIUnknown
Beltone 23348171
FDA UDI
Class IIActive
GN ReSound 20262702
FDA UDI
Class IIUnknown
GN ReSound 20580301
FDA UDI
Class IIUnknown
Beltone 23088900
FDA UDI
Class IIActive
GN ReSound 19705914
FDA UDI
Class IIUnknown
Beltone 19704801
FDA UDI
Class IIUnknown
GN ReSound 20289300
FDA UDI
Class IIUnknown
GN ReSound 21657417
FDA UDI
Class IIUnknown
GN Hearing 22007105
FDA UDI
Class IIActive
Beltone 22083173
FDA UDI
Class IIUnknown
GN ReSound OP604244
FDA UDI
Class IIUnknown
GN ReSound 20932322
FDA UDI
Class IIUnknown
Beltone 22083574
FDA UDI
Class IIUnknown
Beltone TST17ITC-W-HP
FDA UDI
Class IIUnknown
Beltone 19421111
FDA UDI
Class IIUnknown
GN ReSound 18342109
FDA UDI
Class IIUnknown
GN ReSound 20307620
FDA UDI
Class IIUnknown
GN ReSound 19706809
FDA UDI
Class IIUnknown
GN ReSound 18289410
FDA UDI
Class IIUnknown
GN ReSound 20597104
FDA UDI
Class IIUnknown
GN Hearing 23216770
FDA UDI
Class IIActive
GN ReSound 20307608
FDA UDI
Class IIUnknown
GN Hearing 23216275
FDA UDI
Class IIActive
GN Hearing 21878809
FDA UDI
Class IActive
GN ReSound 19196518
FDA UDI
Class IIUnknown
GN ReSound 20591805
FDA UDI
Class IIUnknown
Beltone AY3ITC-DW-MP
FDA UDI
Class IIUnknown
GN ReSound 19196606
FDA UDI
Class IIUnknown
Beltone 18302212
FDA UDI
Class IIUnknown
Beltone 18267920
FDA UDI
Class IIUnknown
GN ReSound 19820200
FDA UDI
Class IUnknown
Beltone IMP9CIC-HP
FDA UDI
Class IActive
Beltone 15345100
FDA UDI
Class IIUnknown
Beltone 20344605
FDA UDI
Class IIUnknown
GN ReSound 23347777
FDA UDI
Class IIActive
GN Hearing PK7ITE-DW-UP
FDA UDI
Class IIUnknown
GN ReSound 18308420
FDA UDI
Class IIUnknown
GN Hearing 22005705
FDA UDI
Class IIActive
GN Hearing 22007504
FDA UDI
Class IIActive
GN ReSound 19420402
FDA UDI
Class IIUnknown
GN ReSound CL8ITC-D-LP
FDA UDI
Class IUnknown
Beltone 20739909
FDA UDI
Class IIActive
GN ReSound 20333602
FDA UDI
Class IIUnknown
GN ReSound 20313702
FDA UDI
Class IIUnknown
GN ReSound 20256320
FDA UDI
Class IIUnknown
Beltone 23369573
FDA UDI
Class IIActive
GN Hearing 23546088
FDA UDI
Class IIActive
GN Hearing 22015772
FDA UDI
Class IIActive
GN ReSound VO730-MUW
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