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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 39 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 23216970
FDA UDI
Class IIActive
GN ReSound 22037400
FDA UDI
Class IIUnknown
GN ReSound 20647906
FDA UDI
Class IIActive
GN ReSound 22345400
FDA UDI
Class IIActive
GN ReSound 21015001
FDA UDI
Class IIActive
GN ReSound 22788772
FDA UDI
Class IIActive
Beltone TST6ITC-W-LP
FDA UDI
Class IIUnknown
GN ReSound 20536609
FDA UDI
Class IIUnknown
GN Hearing 23546086
FDA UDI
Class IIActive
Beltone 19212811
FDA UDI
Class IIUnknown
GN ReSound 19209314
FDA UDI
Class IIUnknown
GN ReSound LT7ITC-D-UP
FDA UDI
Class IUnknown
Beltone 19421008
FDA UDI
Class IIUnknown
GN ReSound 19208704
FDA UDI
Class IIUnknown
GN Hearing XD5CIC-HP
FDA UDI
Class IActive
GN ReSound 21303973
FDA UDI
Class IIUnknown
Beltone 20344550
FDA UDI
Class IIUnknown
GN ReSound 20449614
FDA UDI
Class IIUnknown
Beltone 19185401
FDA UDI
Class IUnknown
GN Hearing 21148574
FDA UDI
Class IIUnknown
GN Hearing 21641500
FDA UDI
Class IActive
GN ReSound 20359809
FDA UDI
Class IIUnknown
GN Hearing 23216571
FDA UDI
Class IIActive
GN ReSound 21193910
FDA UDI
Class IIActive
GN Hearing 23546288
FDA UDI
Class IIActive
Beltone 18710402
FDA UDI
Class IIUnknown
Beltone 22092976
FDA UDI
Class IIUnknown
GN Hearing 18627000
FDA UDI
Class IIActive
GN ReSound 22393600
FDA UDI
Class IIActive
GN ReSound 20460129
FDA UDI
Class IIUnknown
GN ReSound 18883201
FDA UDI
Class IIUnknown
GN ReSound 21435511
FDA UDI
Class IIActive
GN Hearing 23546976
FDA UDI
Class IIActive
GN ReSound 19084820
FDA UDI
Class IIUnknown
GN Hearing 22821074
FDA UDI
Class IIActive
GN Hearing 22020002
FDA UDI
Class IIActive
GN ReSound 21435709
FDA UDI
Class IIActive
Beltone TST17CIC-UP
FDA UDI
Class IUnknown
GN Hearing 20267400
FDA UDI
Class IIUnknown
GN ReSound 20686306
FDA UDI
Class IIActive
GN ReSound 20648010
FDA UDI
Class IIActive
GN ReSound 20597118
FDA UDI
Class IIUnknown
GN ReSound 20460520
FDA UDI
Class IIUnknown
GN Hearing 22928100
FDA UDI
Class IIActive
GN ReSound 20597310
FDA UDI
Class IIUnknown
GN ReSound 18654302
FDA UDI
Class IIUnknown
GN Hearing 23216972
FDA UDI
Class IIActive
GN ReSound 22081376
FDA UDI
Class IIUnknown
GN Hearing 22056800
FDA UDI
Class IIUnknown
GN ReSound 18290020
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