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 40 of 232
DeviceModel / ReferenceRegistriesClassStatus
GN Hearing 21265932
FDA UDI
Class IIUnknown
GN ReSound 19209325
FDA UDI
Class IIUnknown
GN Hearing 23216173
FDA UDI
Class IIActive
Beltone 22366876
FDA UDI
Class IIActive
GN ReSound PZ8MIH-W-MP
FDA UDI
Class IIActive
GN Hearing 22268500
FDA UDI
Class IIActive
Beltone AMZ6MIH-W-HP
FDA UDI
Class IIActive
GN ReSound 21211532
FDA UDI
Class IIActive
GN ReSound 20457004
FDA UDI
Class IIUnknown
GN Hearing 21249309
FDA UDI
Class IIUnknown
GN Hearing 20290600
FDA UDI
Class IIActive
GN ReSound 21225851
FDA UDI
Class IIActive
GN ReSound RE7MIH-WT-HP
FDA UDI
Class IIActive
GN ReSound 19091505
FDA UDI
Class IIUnknown
GN ReSound 19196808
FDA UDI
Class IIUnknown
Beltone 18882000
FDA UDI
Class IUnknown
GN Hearing PK9ITC-D-UP
FDA UDI
Class IUnknown
GN ReSound 21569800
FDA UDI
Class IIActive
GN ReSound 22143770
FDA UDI
Class IIUnknown
GN Hearing 22006520
FDA UDI
Class IIActive
GN Hearing 22503577
FDA UDI
Class IIActive
GN ReSound 20536801
FDA UDI
Class IIUnknown
GN ReSound 21495704
FDA UDI
Class IIActive
Beltone AY2ITE-DW-HP
FDA UDI
Class IIUnknown
Beltone 21340474
FDA UDI
Class IIUnknown
GN Hearing 20268700
FDA UDI
Class IIUnknown
Beltone 21581304
FDA UDI
Class IIActive
Beltone 22083675
FDA UDI
Class IIUnknown
GN Hearing 20291700
FDA UDI
Class IIActive
Beltone TST17MIH-S-HP
FDA UDI
Class IUnknown
Beltone 21582520
FDA UDI
Class IIActive
GN Hearing 22821876
FDA UDI
Class IIActive
GN Hearing 22032400
FDA UDI
Class IIUnknown
GN ReSound 21497104
FDA UDI
Class IIActive
GN ReSound 18666902
FDA UDI
Class IIUnknown
Beltone 19628308
FDA UDI
Class IIUnknown
GN Hearing 23547071
FDA UDI
Class IIActive
GN Hearing 22982576
FDA UDI
Class IIActive
GN ReSound 21630608
FDA UDI
Class IIActive
GN ReSound 21223100
FDA UDI
Class IIActive
GN Hearing 23546872
FDA UDI
Class IIActive
GN ReSound 21496305
FDA UDI
Class IIActive
GN ReSound 20550710
FDA UDI
Class IIUnknown
GN ReSound 19195701
FDA UDI
Class IIUnknown
GN Hearing 22147970
FDA UDI
Class IIActive
GN Hearing 22006502
FDA UDI
Class IIActive
GN ReSound 23347273
FDA UDI
Class IIActive
GN Hearing 20619801
FDA UDI
Class IIUnknown
GN ReSound 20257432
FDA UDI
Class IIUnknown
GN Hearing 22015870
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