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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 18 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 19861320
FDA UDI
Class IIUnknown
GN ReSound 19366200
FDA UDI
Class IUnknown
GN ReSound 23369471
FDA UDI
Class IIActive
GN ReSound 22835374
FDA UDI
Class IIActive
GN ReSound 22619700
FDA UDI
Class IActive
GN Hearing 23216570
FDA UDI
Class IIActive
GN Hearing PM8ITC-DWC-MP
FDA UDI
Class IIActive
Beltone 21304171
FDA UDI
Class IIUnknown
Beltone 19397250
FDA UDI
Class IIUnknown
Beltone 21147874
FDA UDI
Class IIUnknown
GN ReSound 21190405
FDA UDI
Class IIActive
GN Hearing PKX9ITC-LP
FDA UDI
Class IUnknown
GN ReSound 20558502
FDA UDI
Class IIUnknown
Beltone 18267409
FDA UDI
Class IIUnknown
GN Hearing 22986372
FDA UDI
Class IIActive
GN Hearing 22822677
FDA UDI
Class IIActive
Beltone 19705304
FDA UDI
Class IIUnknown
GN Hearing 22986370
FDA UDI
Class IIActive
GN Hearing 22161901
FDA UDI
Class IIActive
Beltone 21881000
FDA UDI
Class IIUnknown
GN ReSound 21630602
FDA UDI
Class IIActive
Beltone AMZ6CIC-W-LP
FDA UDI
Class IIActive
GN ReSound LS5CIC-LP
FDA UDI
Class IUnknown
GN Hearing 21266005
FDA UDI
Class IIUnknown
Beltone 19703408
FDA UDI
Class IIUnknown
Beltone 17862109
FDA UDI
Class IIUnknown
GN ReSound 18404702
FDA UDI
Class IUnknown
GN Hearing 22147670
FDA UDI
Class IIActive
GN Hearing 20293500
FDA UDI
Class IIActive
GN ReSound VOT930-DPW
FDA UDI
Class IIUnknown
GN Hearing 23545372
FDA UDI
Class IIActive
GN ReSound 19227509
FDA UDI
Class IIUnknown
GN Hearing 23385600
FDA UDI
Class IIActive
GN ReSound 18288220
FDA UDI
Class IIUnknown
GN Hearing 21989900
FDA UDI
Class IIUnknown
GN ReSound 21495702
FDA UDI
Class IIActive
Beltone 18972601
FDA UDI
Class IIUnknown
GN ReSound 21763000
FDA UDI
Class IIActive
GN ReSound 20647952
FDA UDI
Class IIActive
GN Hearing 21003104
FDA UDI
Class IIUnknown
Beltone 21331209
FDA UDI
Class IIActive
GN ReSound FT6ITC-UP
FDA UDI
Class IUnknown
GN ReSound 20460608
FDA UDI
Class IIUnknown
Beltone IMG17ITC-DWC-LP
FDA UDI
Class IIUnknown
GN ReSound 21435802
FDA UDI
Class IIActive
Beltone TST9ITC-D-LP
FDA UDI
Class IUnknown
GN Hearing 509-012-000-00
FDA UDI
Class IIUnknown
GN Hearing 20977602
FDA UDI
Class IIUnknown
Beltone 20673100
FDA UDI
Class IIUnknown
GN ReSound 22081672
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

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Importers

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Notified Bodies

Not available yet.

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