EarQ

G10, Minirite T 312 2.4G C093 Earq

Registry build 21.09.26
4manufacturers in China registered for this device type
17catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (3), Fujian (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KLW
Manufacturer City Province Registered as Device types
GN Resound China, Ltd. Xiamen Fujian Contract manufacturer 7
Sonova Hearing (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 3
Jiangsu Betterlife Medical Co., Ltd. Jiangsu Jiangsu Manufacturer 4
Starkey (Suzhou) Hearing Technology Co., Ltd. Guoxiang, Wuzhong District, Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for EarQ
Listed by Oticon A/S, Denmark
FDA product code KLW
Device type Masker, Tinnitus
Device class Class 2
Regulation 21 CFR 874.3400
Establishment Specification developer, Manufacturer
Record published 2018-08-20
Record revised 2020-10-06 (version 2)

Specifications

Specifications
MRI safety MR Unsafe
Prescription Prescription only
Label carries serial number
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for EarQ
Catalogue number Size Status
193370 In distribution
193366 In distribution
193368 In distribution
193570 In distribution
193373 In distribution
193501 In distribution
193564 In distribution
193374 In distribution
193376 In distribution
193367 In distribution
193492 In distribution
193378 In distribution
193382 In distribution
193571 In distribution
193365 In distribution
193563 In distribution
193498 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Oticon Sbo Hearing A/S 570
Starkey Starkey Laboratories, Inc. 449
Phonak Sonova AG 448
Oticon Oticon A/S 353
Nuear Starkey Laboratories, Inc. 336
Audibel Starkey Laboratories, Inc. 318
Unitron Unitron Hearing Division 292
Audigy Starkey Laboratories, Inc. 284
Microtech Starkey Laboratories, Inc. 284
audifon Audifon – Gmbh & Co.kg 277
Philips Sbo Hearing A/S 270
Agxo Sbo Hearing A/S 260

Showing 12 of 86. All products under Masker, Tinnitus

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K133308 2014-03-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer