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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 20 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 19209605
FDA UDI
Class IIUnknown
GN ReSound 18302416
FDA UDI
Class IIUnknown
GN Hearing 23544871
FDA UDI
Class IIActive
GN ReSound 21225805
FDA UDI
Class IIActive
GN ReSound LT7ITC-HP
FDA UDI
Class IUnknown
GN ReSound 19209604
FDA UDI
Class IIUnknown
GN ReSound LS7ITC-W-UP
FDA UDI
Class IIUnknown
Beltone 18710220
FDA UDI
Class IIUnknown
GN ReSound 20638700
FDA UDI
Class IIUnknown
GN ReSound 20453308
FDA UDI
Class IIUnknown
Beltone 22790274
FDA UDI
Class IIActive
Beltone 22486376
FDA UDI
Class IIActive
Beltone 21214202
FDA UDI
Class IIActive
GN Hearing 21003201
FDA UDI
Class IIUnknown
Beltone 23304774
FDA UDI
Class IIActive
GN Hearing 20782632
FDA UDI
Class IIUnknown
GN Hearing 23531300
FDA UDI
Class IIActive
Beltone TST9ITE-D-HP
FDA UDI
Class IUnknown
GN Hearing 22982671
FDA UDI
Class IIActive
GN Hearing 18501200
FDA UDI
Class IIActive
GN Hearing 19883702
FDA UDI
Class IIUnknown
GN ReSound 19368506
FDA UDI
Class IIUnknown
GN Hearing 23544772
FDA UDI
Class IIActive
GN Hearing 23545671
FDA UDI
Class IIActive
Beltone 22486972
FDA UDI
Class IIActive
Beltone 20673511
FDA UDI
Class IIUnknown
GN Hearing FP9ITE-W-HP
FDA UDI
Class IIUnknown
GN ReSound 20556950
FDA UDI
Class IIUnknown
GN ReSound 20550300
FDA UDI
Class IIUnknown
Beltone RLY4CIC-W-LP
FDA UDI
Class IIActive
GN ReSound 20457302
FDA UDI
Class IIUnknown
GN ReSound 20094652
FDA UDI
Class IIUnknown
GN Hearing 23685875
FDA UDI
Class IIActive
GN ReSound 21190425
FDA UDI
Class IIActive
GN Hearing 19884604
FDA UDI
Class IIUnknown
GN ReSound 18958005
FDA UDI
Class IIUnknown
GN ReSound 18338602
FDA UDI
Class IIUnknown
GN ReSound 19195609
FDA UDI
Class IIUnknown
GN Hearing XC4ITE-DW-HP
FDA UDI
Class IIActive
GN ReSound 21497308
FDA UDI
Class IIActive
Beltone 21214520
FDA UDI
Class IIActive
GN Hearing 22943976
FDA UDI
Class IIActive
Beltone 22366772
FDA UDI
Class IIActive
GN ReSound 21435704
FDA UDI
Class IIActive
Beltone TST6MIH-W-UP
FDA UDI
Class IIUnknown
GN ReSound 19697600
FDA UDI
Class IIUnknown
GN ReSound 19706232
FDA UDI
Class IIUnknown
Beltone 21283300
FDA UDI
Class IActive
GN ReSound LT9MIH-S-HP
FDA UDI
Class IUnknown
Beltone 22366671
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