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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 8 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20316301
FDA UDI
Class IIUnknown
GN Hearing 19884601
FDA UDI
Class IIUnknown
GN ReSound CL8ITC-W-HP
FDA UDI
Class IIUnknown
GN ReSound 18342412
FDA UDI
Class IIUnknown
GN ReSound 20332008
FDA UDI
Class IIUnknown
GN ReSound 19084110
FDA UDI
Class IIUnknown
GN Hearing XF9ITE-DWC-UP
FDA UDI
Class IIActive
GN Hearing 18629900
FDA UDI
Class IIActive
GN ReSound RT5ITC-DWC-HP
FDA UDI
Class IIUnknown
GN Hearing 22020008
FDA UDI
Class IIActive
GN ReSound 20537005
FDA UDI
Class IIUnknown
Beltone 21580304
FDA UDI
Class IIActive
GN ReSound 21435504
FDA UDI
Class IIActive
GN ReSound RU5ITE-DWC-UP
FDA UDI
Class IIActive
Beltone 21582302
FDA UDI
Class IIActive
GN ReSound CL8ITE-W-MP
FDA UDI
Class IIUnknown
GN ReSound 19962620
FDA UDI
Class IIUnknown
GN ReSound RE9CIC-LP
FDA UDI
Class IActive
Beltone 19963309
FDA UDI
Class IIUnknown
GN Hearing 22271277
FDA UDI
Class IIUnknown
GN ReSound 21496605
FDA UDI
Class IIActive
GN ReSound EY3ITC-W-MP
FDA UDI
Class IIUnknown
GN ReSound 20710705
FDA UDI
Class IIUnknown
GN ReSound 21263752
FDA UDI
Class IIActive
GN ReSound 21496520
FDA UDI
Class IIActive
Beltone 21340475
FDA UDI
Class IIUnknown
GN ReSound 20457520
FDA UDI
Class IIUnknown
GN Hearing 22822470
FDA UDI
Class IIActive
GN ReSound 22175871
FDA UDI
Class IIActive
GN ReSound LT5ITC-D-MP
FDA UDI
Class IUnknown
GN Hearing 22008375
FDA UDI
Class IIUnknown
Beltone AY3ITE-D-MP
FDA UDI
Class IUnknown
GN Hearing 22822176
FDA UDI
Class IIActive
GN ReSound 22176173
FDA UDI
Class IIActive
Beltone 22083176
FDA UDI
Class IIUnknown
GN Hearing 22007102
FDA UDI
Class IIActive
GN ReSound LT9ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound 20410100
FDA UDI
Class IIUnknown
Beltone 20393504
FDA UDI
Class IIUnknown
GN ReSound 17587304
FDA UDI
Class IUnknown
Beltone 21606000
FDA UDI
Class IIUnknown
GN ReSound 22789076
FDA UDI
Class IIActive
Beltone 22083372
FDA UDI
Class IIUnknown
GN ReSound 20457409
FDA UDI
Class IIUnknown
GN ReSound 20087601
FDA UDI
Class IIUnknown
Beltone 19316402
FDA UDI
Class IIUnknown
Beltone 17842004
FDA UDI
Class IUnknown
GN ReSound 19091532
FDA UDI
Class IIUnknown
GN ReSound 20967371
FDA UDI
Class IIUnknown
GN Hearing 20967775
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