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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 47 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 23545670
FDA UDI
Class IIActive
GN ReSound 20580101
FDA UDI
Class IIUnknown
GN ReSound 21213801
FDA UDI
Class IIActive
GN ReSound 22835174
FDA UDI
Class IIActive
GN ReSound 21196408
FDA UDI
Class IIActive
GN Hearing 23545576
FDA UDI
Class IIActive
Beltone 23369874
FDA UDI
Class IIActive
GN ReSound 21213520
FDA UDI
Class IIActive
GN ReSound 20574215
FDA UDI
Class IIUnknown
GN Hearing 22236400
FDA UDI
Class IIUnknown
GN ReSound 20967372
FDA UDI
Class IIUnknown
GN ReSound 19208718
FDA UDI
Class IIUnknown
GN Hearing 22975971
FDA UDI
Class IIActive
GN Hearing 22019702
FDA UDI
Class IIActive
GN Hearing FP9CIC-UP
FDA UDI
Class IUnknown
Beltone 20967875
FDA UDI
Class IIUnknown
GN Hearing 21432000
FDA UDI
Class IIActive
GN ReSound 21213832
FDA UDI
Class IIActive
GN Hearing 22822171
FDA UDI
Class IIActive
GN Hearing 22148473
FDA UDI
Class IIActive
Beltone LND6MIH-HP
FDA UDI
Class IUnknown
GN ReSound 19705802
FDA UDI
Class IIUnknown
GN Hearing 23546871
FDA UDI
Class IIActive
Beltone 19397201
FDA UDI
Class IIUnknown
GN Hearing 22277371
FDA UDI
Class IIActive
GN Hearing PKX7ITE-D-MP
FDA UDI
Class IUnknown
GN ReSound 20993100
FDA UDI
Class IIActive
GN ReSound 19078851
FDA UDI
Class IIUnknown
GN ReSound 19396918
FDA UDI
Class IIUnknown
GN ReSound 18876102
FDA UDI
Class IUnknown
GN Hearing 21881600
FDA UDI
Class IIUnknown
GN Hearing 23384700
FDA UDI
Class IIActive
GN ReSound 20537301
FDA UDI
Class IIUnknown
GN Hearing 18628200
FDA UDI
Class IIActive
Beltone 20648209
FDA UDI
Class IIActive
GN ReSound 19705806
FDA UDI
Class IIUnknown
GN Hearing 23685771
FDA UDI
Class IIActive
GN ReSound 21310702
FDA UDI
Class IIActive
Beltone 21264209
FDA UDI
Class IIActive
GN ReSound 20556952
FDA UDI
Class IIUnknown
Beltone 21189300
FDA UDI
Class IActive
GN ReSound Y3ITC-W-MP
FDA UDI
Class IIUnknown
GN Hearing 20780804
FDA UDI
Class IIUnknown
GN ReSound 20536509
FDA UDI
Class IIUnknown
GN ReSound LS9CIC-UP
FDA UDI
Class IUnknown
GN ReSound 20460205
FDA UDI
Class IIUnknown
GN Hearing 20265801
FDA UDI
Class IIUnknown
GN ReSound 20460609
FDA UDI
Class IIUnknown
GN Hearing 20366702
FDA UDI
Class IIUnknown
Beltone 21211805
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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Importers

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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