Flexal

Cardinal Health Glove Exam NON-Sterile Nitrile Flexal Biodegradable Powder-Free Extra Large

Registry build 21.09.26
83manufacturers in China registered for this device type
32catalogue numbers in this listing
5recalls on this code

Who Else Makes It

Concentrated in Shandong (27), Guangdong (10), Jiangsu (8). 11 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LZA
Manufacturer City Province Registered as Device types
YUE Kang Anhui Medical Products Co., Ltd. Huaibei Anhui Contract manufacturer 5
Opus Gloves Co., Ltd. Shanghai Shanghai Contract manufacturer 5
Better Care Plastic Technology Co., Ltd. Shenze County Hebei Contract manufacturer 4
Xingyu Medical Tech Co., Ltd. Weifang Shandong Contract manufacturer 4
Lingshi Hongruida Health Protection Technology Co., Ltd. Jinzhong Shanxi Contract manufacturer 4
Zhangjiagang Blackbox Plastic Products Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 4
Zhangjiagang Dayu Rubber Products Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 4
Xuzhou Full Sun Medical Products Ltd. Pizhou Jiangsu Contract manufacturer 3
Zhongnuo Medical Products Co., Ltd. Tangshan Hebei Contract manufacturer 3
Anhui Kindguard Medical Supplies Technology Co., Ltd. Suzhou Anhui Contract manufacturer 2
Puyang Linshi Medical Supplies Co., Ltd. Puyang Henan Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146

Showing 12 of 83. All 83 manufacturers in China registered for Polymer Patient Examination Glove

Record

Regulatory record for Flexal
Listed by Cardinal Health 200, LLC, United States
FDA product code LZA
Device type Polymer Patient Examination Glove
Device class Class 1
Regulation 21 CFR 880.6250
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2019-03-06
Record revised 2024-09-26 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Over the counter Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date, manufacturing date
Packaging Case of 10, case of 20, case of 100
Distribution end date 2021-12-31

Catalogue Numbers

Catalogue numbers for Flexal
Catalogue number Size Per pack Status
88FS04L 250 In distribution
88FS02S 250 In distribution
88FS 10 In distribution
88RT02S 250 In distribution
88TN06XXL 200 In distribution
88RT06XXL 230 In distribution
88TN02S 200 In distribution
88FB03M 200 In distribution
88FB02S 200 In distribution
88TN03M 200 In distribution
88FB05XL 200 In distribution
88TN04L 200 In distribution
88TN01XS 200 In distribution
88RT100L 100 In distribution
88RT100XS 100 In distribution
88RT03M 250 In distribution
88TN05XL 200 In distribution
88TNF03M 200 Withdrawn
88TNF02S 200 Withdrawn
88TNF04L 200 Withdrawn
N88TT23L 100 Withdrawn
N88TT24XL 100 Withdrawn
88TT24XL 250 Withdrawn
88TT20XS 300 Withdrawn
88TNF06XXL 200 Withdrawn
N88TT22M 100 Withdrawn
88TT23L 300 Withdrawn
88TNF01XS 200 Withdrawn
88TNF05XL 200 Withdrawn
88TT21S 300 Withdrawn
88TT22M 300 Withdrawn
N88TT21S 100 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Medline Medline Industries, Inc. 255
Microflex Ansell Healthcare Product 185
FifthPulse Jeg & Sons Inc. 135
SW SW Safety Solutions Inc. 130
Halyard O&M Halyard, Inc. 120
Basic Intco Medical Industries, Inc. 119
Cranberry Ascend Eagle, Inc. 109
1st Choice Ammex Corporation 101
JMU JMU Dental, Inc 90
Vivit Supply Vivit Supply LLC 86
McKesson Mckesson Medical-Surgical Inc. 75
Natural Extensions Benco Dental Supply Co. 74

Showing 12 of 930. All products under Polymer Patient Examination Glove

Recalls

5 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2019-03-22 Class II Nonconforming Material/Component Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap 3236 2021-08-06
2019-03-22 Class II Nonconforming Material/Component Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap 5415 2021-08-06
2019-03-22 Class II Nonconforming Material/Component Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap 11588 2021-08-06
2019-03-22 Class II Nonconforming Material/Component Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap 21082 2021-08-06
2015-08-25 Class II Nonconforming Material/Component Ambitex Nitrile NMD400 Exam Gloves size medium on exam hold were inadvertently placed into commerce. The product was under Exam Hold because samples pulled from a shipment manufactured by the firm failed the water leak test performed by FDA 34 cases. 2016-08-01

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