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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 45 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 20580111
FDA UDI
Class IIUnknown
GN ReSound 19396908
FDA UDI
Class IIUnknown
GN ReSound 21631002
FDA UDI
Class IIActive
GN ReSound 22835573
FDA UDI
Class IIActive
GN ReSound LS7ITE-MP
FDA UDI
Class IUnknown
GN ReSound Y3ITC-DW-MP
FDA UDI
Class IIUnknown
GN ReSound 20333608
FDA UDI
Class IIUnknown
GN Hearing CH950-W
FDA UDI
Class IIUnknown
Beltone AY2ITC-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 21266025
FDA UDI
Class IIUnknown
GN Hearing 511-002-000-01
FDA UDI
Class IIUnknown
GN ReSound Y2ITC-DW-UP
FDA UDI
Class IIUnknown
GN ReSound L7ITC-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 19398500
FDA UDI
Class IIActive
GN ReSound 20262801
FDA UDI
Class IIUnknown
GN ReSound 22216100
FDA UDI
Class IIUnknown
GN ReSound 20648025
FDA UDI
Class IIActive
Beltone TST9CIC-LP
FDA UDI
Class IUnknown
Beltone TST17CIC-MP
FDA UDI
Class IUnknown
GN ReSound 22081276
FDA UDI
Class IIUnknown
GN Hearing 22982776
FDA UDI
Class IIActive
GN ReSound 22082177
FDA UDI
Class IIUnknown
GN Hearing 22148173
FDA UDI
Class IIActive
GN ReSound 20413932
FDA UDI
Class IIActive
Beltone AY3ITE-W-UP
FDA UDI
Class IIUnknown
GN ReSound 19877902
FDA UDI
Class IIUnknown
Beltone 19208911
FDA UDI
Class IIUnknown
GN ReSound 19191425
FDA UDI
Class IIUnknown
GN ReSound 18338502
FDA UDI
Class IIUnknown
Beltone IMP6ITE-DWC-UP
FDA UDI
Class IIActive
GN Hearing OP603908
FDA UDI
Class IIUnknown
GN ReSound 18288006
FDA UDI
Class IIUnknown
GN ReSound 20591509
FDA UDI
Class IIUnknown
GN Hearing 20367202
FDA UDI
Class IIUnknown
GN ReSound 22495500
FDA UDI
Class IIActive
Beltone 23369671
FDA UDI
Class IIActive
Beltone 20344505
FDA UDI
Class IIUnknown
GN ReSound 23098477
FDA UDI
Class IIActive
GN ReSound 20359808
FDA UDI
Class IIUnknown
GN ReSound 21435604
FDA UDI
Class IIActive
GN ReSound 21435808
FDA UDI
Class IIActive
GN ReSound RU9ITC-DWC-HP
FDA UDI
Class IIActive
GN ReSound 19698600
FDA UDI
Class IIUnknown
GN ReSound LS5ITC-DW-HP
FDA UDI
Class IIUnknown
GN Hearing 20265204
FDA UDI
Class IIUnknown
Beltone 21211804
FDA UDI
Class IIActive
Beltone 23305071
FDA UDI
Class IIActive
Beltone 19785200
FDA UDI
Class IUnknown
GN Hearing 23760475
FDA UDI
Class IIActive
GN ReSound 18338301
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