Sonova Brand (Multiple Brand)

All-Day Clear Slim ADCS1 demo (US)

Registry build 21.09.26
4manufacturers in China registered for this device type
3catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (2), Fujian (1), Guangdong (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 QUH
Manufacturer City Province Registered as Device types
Luxshare Electronic Technology (Kunshan) Ltd. Kunshan Jiangsu Contract manufacturer 1
Maintek Computer (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 1
GN Resound China, Ltd. Xiamen Fujian Contract manufacturer 7
Huizhou Jinghao Medical Technology Co., Ltd. Huizhou Guangdong Contract manufacturer 5

Record

Regulatory record for Sonova Brand (multiple brand)
Listed by Sonova AG, Switzerland
FDA product code QUH
Device type Self-Fitting Air-Conduction Hearing Aid, Over The Counter
Device class Class 2
Regulation 21 CFR 874.3325
Establishment Specification developer, Manufacturer
Record published 2022-12-12
Record revised 2026-04-15 (version 5)

Specifications

Specifications
MRI safety MR Unsafe
Over the counter Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Sonova Brand (multiple brand)
Catalogue number Size Status
051-5047-AB In distribution
051-5107-AB In distribution
051-5046-AB In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Eargo SE Eargo Inc 16
Soundwave Hearing Soundwave Hearing, LLC 14
GN Hearing GN Hearing A/S 13
Sontro Self-Fitting OTC Hearing Aids Soundwave Hearing, LLC 12
Eargo 5 Eargo Inc 12
Eargo 8 Eargo Inc 11
Lexie Hearing Hearx SA 11
Sony WS Audiology USA, Inc. 5
Eargo 6 Eargo Inc 3
Eargo 7 Eargo Inc 3
Audialnet Huizhou Jinghao Medical Technology Co., Ltd. 2
hear.com WS Audiology USA, Inc. 2

Showing 12 of 28. All products under Self-Fitting Air-Conduction Hearing Aid, Over The Counter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K230538 2023-06-16

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