Quality Choice

Quality Choice Contact Lens Case - 2 Count

Registry build 21.09.26
6manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Shanghai (2), Guangdong (2), elsewhere (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code LRX
Manufacturer City Province Registered as Device types
Shun SZE Industrial (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 22
China (Shenyang) MED-Land IMP/EXP Corp., Ltd. Shanghai Shanghai Exporter 32
Shanghai Care Us Medical Product Co., Ltd. Shanghai Shanghai Contract manufacturer 30
Action Eyewear Corp. Dong Guan Guangdong Contract manufacturer 5
Ningbo Kaida Rubber AND Plastic Technology Co., Ltd. Yu Yao City, Zhejiang Province Contract manufacturer 2
Danyang Chanxin Glasses Cases Factory Danyang Jiangsu Manufacturer 1

Record

Regulatory record for Quality Choice
Listed by Sacks Holdings, Inc., United States
FDA product code LRX
Device type Case, Contact Lens
Device class Class 2
Regulation 21 CFR 886.5928
Establishment Repacker / relabeller
Record published 2024-03-28

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Quality Choice
Catalogue number Size Status
00635515966918 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Optisource Phoenix Medical Solutions 18
Bonasse Bonasse Enterprises Co., Ltd. 12
Equate Wal Mart Stores, Inc 11
Optego Optego Vision USA, Inc. 10
UP & UP Target Health, Inc. 7
Meijer Meijer, Inc. 6
Flents Apothecary Products, LLC. 6
Jingsheng Ningbo Haishu Jingsheng Plastic Co., Ltd. 4
Bausch + Lomb Bausch & Lomb Incorporated 4
Apex Drive DeVilbiss Healthcare 3
Color Case Watchdog Group, LC 3
Phoenix Healthcare Solutions LLC Phoenix Medical Solutions 3

Showing 12 of 52. All products under Case, Contact Lens

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K121030 2012-07-06

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