Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 43 of 232
DeviceModel / ReferenceRegistriesClassStatus
Beltone 19368804
FDA UDI
Class IIUnknown
Beltone 21581505
FDA UDI
Class IIActive
GN Hearing 19883701
FDA UDI
Class IIUnknown
Beltone 23348470
FDA UDI
Class IIActive
GN ReSound 22834973
FDA UDI
Class IIActive
GN Hearing 22976171
FDA UDI
Class IIActive
Beltone 22486870
FDA UDI
Class IIActive
GN ReSound 21496505
FDA UDI
Class IIActive
GN ReSound 20314052
FDA UDI
Class IIUnknown
Beltone 21582309
FDA UDI
Class IIActive
GN Hearing 22982574
FDA UDI
Class IIActive
GN ReSound 22176171
FDA UDI
Class IIActive
GN ReSound 21175400
FDA UDI
Class IActive
GN Hearing 22039300
FDA UDI
Class IIUnknown
GN Hearing 20279700
FDA UDI
Class IIUnknown
GN Hearing 22821877
FDA UDI
Class IIActive
GN Hearing 18777800
FDA UDI
Class IIUnknown
GN Hearing 21989700
FDA UDI
Class IIUnknown
GN Hearing 21003020
FDA UDI
Class IIUnknown
GN Hearing 23370178
FDA UDI
Class IIActive
GN Hearing 20782718
FDA UDI
Class IIUnknown
GN ReSound 21398400
FDA UDI
Class IIActive
GN ReSound RE7MIH-WT-MP
FDA UDI
Class IIActive
GN Hearing 20780806
FDA UDI
Class IIUnknown
GN Hearing 22269575
FDA UDI
Class IIUnknown
GN Hearing 21741008
FDA UDI
Class IIActive
GN Hearing 23371100
FDA UDI
Class IIActive
GN Hearing 20782714
FDA UDI
Class IIUnknown
GN Hearing 23546371
FDA UDI
Class IIActive
GN Hearing 23545379
FDA UDI
Class IIActive
GN Hearing 23315476
FDA UDI
Class IIActive
Beltone 21214205
FDA UDI
Class IIActive
GN ReSound 20580320
FDA UDI
Class IIUnknown
Beltone SER9CIC-HP
FDA UDI
Class IActive
GN Hearing 22976272
FDA UDI
Class IIActive
GN ReSound 19706708
FDA UDI
Class IIUnknown
GN Hearing 20274900
FDA UDI
Class IIUnknown
GN Hearing 23370078
FDA UDI
Class IIActive
GN Hearing 21432700
FDA UDI
Class IIActive
GN ReSound 20686310
FDA UDI
Class IIActive
GN ReSound 20267100
FDA UDI
Class IUnknown
GN ReSound 20071100
FDA UDI
Class IUnknown
Beltone 19703301
FDA UDI
Class IIUnknown
Beltone 19705008
FDA UDI
Class IIUnknown
GN Hearing 20276600
FDA UDI
Class IIUnknown
GN ReSound KE3CIC-W-MP
FDA UDI
Class IIActive
GN ReSound LT5MIH-W-UP
FDA UDI
Class IIUnknown
GN Hearing 23561600
FDA UDI
Class IIActive
GN Hearing 23373200
FDA UDI
Class IIActive
Beltone 23347970
FDA UDI
Class IIActive

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