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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 38 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 22020320
FDA UDI
Class IIActive
Beltone 21340476
FDA UDI
Class IIUnknown
GN Hearing 21249506
FDA UDI
Class IIUnknown
Beltone 21231208
FDA UDI
Class IIActive
GN ReSound 20597308
FDA UDI
Class IIUnknown
GN Hearing 20367020
FDA UDI
Class IIUnknown
GN Hearing XF7CIC-HP
FDA UDI
Class IActive
GN Hearing 22502075
FDA UDI
Class IIActive
GN ReSound LS9CIC-MP
FDA UDI
Class IUnknown
Beltone 22790071
FDA UDI
Class IIActive
Beltone AMZ17ITC-DW-LP
FDA UDI
Class IIActive
GN ReSound 23175771
FDA UDI
Class IIActive
GN ReSound 21164551
FDA UDI
Class IIActive
GN Hearing 20782610
FDA UDI
Class IIUnknown
GN ReSound 20709801
FDA UDI
Class IIUnknown
GN ReSound 19508609
FDA UDI
Class IIActive
GN Hearing 22270672
FDA UDI
Class IIUnknown
GN Hearing 22148472
FDA UDI
Class IIActive
GN ReSound 20536302
FDA UDI
Class IIUnknown
GN Hearing XF7ITC-DW-UP
FDA UDI
Class IIActive
GN Hearing 22452470
FDA UDI
Class IIActive
GN ReSound 20403325
FDA UDI
Class IIUnknown
Beltone 19368811
FDA UDI
Class IIUnknown
GN ReSound 18929009
FDA UDI
Class IIUnknown
Beltone 23347971
FDA UDI
Class IIActive
GN Hearing FP9ITC-W-MP
FDA UDI
Class IIUnknown
GN ReSound 20580205
FDA UDI
Class IIUnknown
GN Hearing 23576376
FDA UDI
Class IIActive
Beltone 21310409
FDA UDI
Class IIActive
Beltone 23526775
FDA UDI
Class IIActive
GN ReSound 21190402
FDA UDI
Class IIActive
GN Hearing 22503472
FDA UDI
Class IIActive
GN ReSound 21213405
FDA UDI
Class IIActive
GN ReSound RE7ITC-DW-MP
FDA UDI
Class IIActive
GN Hearing PKX9ITC-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 22019720
FDA UDI
Class IIActive
GN Hearing 22822274
FDA UDI
Class IIActive
GN ReSound KE2ITC-DW-UP
FDA UDI
Class IIActive
GN ReSound 20959920
FDA UDI
Class IIActive
Beltone OR235-DP
FDA UDI
Class IUnknown
GN ReSound 20410600
FDA UDI
Class IIActive
GN ReSound 19420808
FDA UDI
Class IIUnknown
Beltone 21180700
FDA UDI
Class IActive
GN ReSound 18741114
FDA UDI
Class IIUnknown
GN Hearing 23760770
FDA UDI
Class IIActive
GN ReSound RU9ITC-DWC-UP
FDA UDI
Class IIActive
Beltone 19785600
FDA UDI
Class IUnknown
GN ReSound 20331502
FDA UDI
Class IIUnknown
GN ReSound 19964401
FDA UDI
Class IIUnknown
GN ReSound 22081374
FDA UDI
Class IIUnknown

Related Companies

Authorised Representatives

No authorised representatives on record.

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