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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 5 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22975777
FDA UDI
Class IIActive
GN Hearing 22267800
FDA UDI
Class IIActive
GN Hearing 19402600
FDA UDI
Class IIUnknown
Beltone 19627700
FDA UDI
Class IIUnknown
GN ReSound RT7ITE-DWC-HP
FDA UDI
Class IIUnknown
GN ReSound 21263801
FDA UDI
Class IIActive
GN ReSound 20537318
FDA UDI
Class IIUnknown
Beltone 23369876
FDA UDI
Class IIActive
GN Hearing PKX9MIH-MP
FDA UDI
Class IUnknown
GN Hearing 21305073
FDA UDI
Class IIUnknown
Beltone 21587500
FDA UDI
Class IIActive
GN Hearing 20620104
FDA UDI
Class IIUnknown
GN ReSound 20344851
FDA UDI
Class IIUnknown
GN ReSound L7ITE-DW-HP
FDA UDI
Class IIUnknown
GN ReSound 20263102
FDA UDI
Class IIUnknown
Beltone 22082970
FDA UDI
Class IIUnknown
Beltone 21185400
FDA UDI
Class IActive
GN Hearing PM8ITC-DWC-HP
FDA UDI
Class IIActive
GN ReSound 19706520
FDA UDI
Class IIUnknown
GN ReSound 20307614
FDA UDI
Class IIUnknown
GN ReSound Y3ITC-W-LP
FDA UDI
Class IIUnknown
GN ReSound 19312652
FDA UDI
Class IIUnknown
GN ReSound RT5ITC-DWC-UP
FDA UDI
Class IIActive
Beltone 22223600
FDA UDI
Class IIUnknown
GN ReSound 19698500
FDA UDI
Class IIUnknown
GN ReSound NX7ITC-DWC-LP
FDA UDI
Class IIActive
GN Hearing EP2CIC-HP
FDA UDI
Class IActive
GN Hearing 22277375
FDA UDI
Class IIActive
GN ReSound 19962420
FDA UDI
Class IIUnknown
Beltone 15767100
FDA UDI
Class IIUnknown
GN Hearing 22007108
FDA UDI
Class IIActive
GN ReSound 21230701
FDA UDI
Class IIActive
GN ReSound 21175900
FDA UDI
Class IActive
Beltone TST6MIH-LP
FDA UDI
Class IUnknown
GN Hearing 22020020
FDA UDI
Class IIActive
GN Hearing 22271172
FDA UDI
Class IIUnknown
GN ReSound 20537006
FDA UDI
Class IIUnknown
GN Hearing 23760370
FDA UDI
Class IIActive
GN Hearing 21655100
FDA UDI
Class IIActive
GN ReSound 19078801
FDA UDI
Class IIUnknown
GN ReSound 19195714
FDA UDI
Class IIUnknown
Beltone 19376600
FDA UDI
Class IUnknown
GN ReSound LT7ITE-DW-HP
FDA UDI
Class IIUnknown
Beltone TST17ITE-D-UP
FDA UDI
Class IUnknown
GN Hearing 22147572
FDA UDI
Class IIActive
GN ReSound 22143474
FDA UDI
Class IIUnknown
Beltone TST9MIH-W-MP
FDA UDI
Class IIUnknown
Beltone AMZ9CIC-HP
FDA UDI
Class IActive
GN ReSound 18929010
FDA UDI
Class IIUnknown
GN ReSound 18289401
FDA UDI
Class IIUnknown

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