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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 41 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN ReSound 19368304
FDA UDI
Class IIUnknown
GN ReSound 21435501
FDA UDI
Class IIActive
GN ReSound 22788876
FDA UDI
Class IIActive
GN Hearing 23760279
FDA UDI
Class IIActive
GN Hearing 22516173
FDA UDI
Class IIActive
GN Hearing 21249432
FDA UDI
Class IIUnknown
Beltone TST9ITC-UP
FDA UDI
Class IUnknown
GN Hearing 510-004-100-02O
FDA UDI
Class IIUnknown
GN Hearing 18655500
FDA UDI
Class IIActive
GN ReSound FT6ITE-D-MP
FDA UDI
Class IUnknown
GN ReSound 19209709
FDA UDI
Class IIUnknown
GN Hearing 22985971
FDA UDI
Class IIActive
GN Hearing 22821071
FDA UDI
Class IIActive
GN ReSound 20536909
FDA UDI
Class IIUnknown
GN Hearing 23547375
FDA UDI
Class IIActive
GN ReSound 18929014
FDA UDI
Class IIUnknown
GN ReSound 18741110
FDA UDI
Class IIUnknown
GN ReSound 19190214
FDA UDI
Class IIUnknown
Beltone 22339873
FDA UDI
Class IIActive
GN Hearing 23546085
FDA UDI
Class IIActive
GN Hearing 23545071
FDA UDI
Class IIActive
GN Hearing 22006608
FDA UDI
Class IIActive
GN ReSound 21637700
FDA UDI
Class IIUnknown
GN ReSound 20647814
FDA UDI
Class IIActive
GN ReSound 20708920
FDA UDI
Class IIUnknown
GN Hearing 20426402
FDA UDI
Class IIUnknown
GN Hearing 22977575
FDA UDI
Class IIActive
GN ReSound 19195604
FDA UDI
Class IIUnknown
GN ReSound 16861900
FDA UDI
Class IIUnknown
GN ReSound 19360200
FDA UDI
Class IUnknown
Beltone 22789974
FDA UDI
Class IIActive
Beltone 21580904
FDA UDI
Class IIActive
Beltone 22083576
FDA UDI
Class IIUnknown
GN ReSound LT7ITC-W-UP
FDA UDI
Class IIUnknown
GN ReSound 20739020
FDA UDI
Class IIActive
Beltone 19784000
FDA UDI
Class IUnknown
GN Hearing 20993700
FDA UDI
Class IIActive
GN Hearing 23530600
FDA UDI
Class IIActive
GN Hearing FP7ITE-W-HP
FDA UDI
Class IIUnknown
GN Hearing 21397001
FDA UDI
Class IIUnknown
GN ReSound 21211632
FDA UDI
Class IIActive
GN Hearing 23366970
FDA UDI
Class IIActive
GN Hearing 20782520
FDA UDI
Class IIUnknown
GN Hearing 22019620
FDA UDI
Class IIActive
GN ReSound 20074100
FDA UDI
Class IUnknown
GN Hearing FP9ITE-D-UP
FDA UDI
Class IUnknown
GN Hearing 22985672
FDA UDI
Class IIActive
GN Hearing 23179574
FDA UDI
Class IIActive
GN ReSound 23120000
FDA UDI
Class IIActive
GN ReSound 20558604
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