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 16 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 23216775
FDA UDI
Class IIActive
Beltone IMG6CIC-MP
FDA UDI
Class IUnknown
GN Hearing 21342977
FDA UDI
Class IIUnknown
GN ReSound 20591402
FDA UDI
Class IIUnknown
Beltone 19703305
FDA UDI
Class IIUnknown
GN Hearing 22006008
FDA UDI
Class IIActive
GN ReSound LT7ITE-DW-MP
FDA UDI
Class IIUnknown
GN ReSound CL8ITE-DW-UP
FDA UDI
Class IIUnknown
GN Hearing 20293100
FDA UDI
Class IIActive
GN ReSound 21538874
FDA UDI
Class IIUnknown
Beltone 22082474
FDA UDI
Class IIUnknown
GN Hearing 22018872
FDA UDI
Class IIUnknown
GN ReSound 20686318
FDA UDI
Class IIActive
GN ReSound 20262201
FDA UDI
Class IIUnknown
GN ReSound 20087608
FDA UDI
Class IIUnknown
GN ReSound 18305504
FDA UDI
Class IIUnknown
Beltone SER6ITE-DWC-HP
FDA UDI
Class IIActive
GN Hearing 22017300
FDA UDI
Class IIActive
GN Hearing 21642800
FDA UDI
Class IActive
GN Hearing 18629600
FDA UDI
Class IIActive
GN ReSound 20591818
FDA UDI
Class IIUnknown
GN ReSound 20537405
FDA UDI
Class IIUnknown
GN ReSound FT8ITE-D-UP
FDA UDI
Class IUnknown
GN Hearing PKX7CIC-UP
FDA UDI
Class IUnknown
GN ReSound 22339673
FDA UDI
Class IIActive
Beltone AMZ9MIH-WT-UP
FDA UDI
Class IIActive
GN ReSound 17841702
FDA UDI
Class IUnknown
GN ReSound 22176577
FDA UDI
Class IIActive
GN ReSound 21881900
FDA UDI
Class IIUnknown
GN ReSound 20686206
FDA UDI
Class IIActive
Beltone 19398002
FDA UDI
Class IIUnknown
GN Hearing 23576775
FDA UDI
Class IIActive
GN ReSound 21311702
FDA UDI
Class IIActive
Beltone 21264409
FDA UDI
Class IIActive
GN ReSound NX5ITE-DWC-MP
FDA UDI
Class IIActive
GN ReSound 19706318
FDA UDI
Class IIUnknown
GN Hearing 22441700
FDA UDI
Class IIActive
GN Hearing 21945590
FDA UDI
Class IIActive
GN ReSound 23369479
FDA UDI
Class IIActive
Beltone 22833676
FDA UDI
Class IIActive
Beltone 21264402
FDA UDI
Class IIActive
GN ReSound 19706506
FDA UDI
Class IIUnknown
Beltone 19703801
FDA UDI
Class IIUnknown
GN ReSound 19705709
FDA UDI
Class IIUnknown
GN Hearing 19883704
FDA UDI
Class IIUnknown
Beltone 22790374
FDA UDI
Class IIActive
GN Hearing 22821077
FDA UDI
Class IIActive
GN ReSound 22176574
FDA UDI
Class IIActive
GN ReSound 22176576
FDA UDI
Class IIActive
GN ReSound 19861250
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