Kendall

Kendall Calcium Alginate Dressing 6 x 10 in. (15.2 x 25.4 cm)

Registry build 21.09.26
3manufacturers in China registered for this device type
15catalogue numbers in this listing
1recall

Who Else Makes It

Concentrated in Guangdong (2), Jiangsu (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 KMF
Manufacturer City Province Registered as Device types
Derma Sciences Nantong Incorporation Development Jiangsu Contract manufacturer 19
Huizhou Foryou Medical Devices Co., Ltd. Huizhou Guangdong Contract manufacturer 18
Shenzhen JPY ION-Tech. Co., Ltd. Shenzhen Guangdong Contract manufacturer 20

Record

Regulatory record for Kendall
Listed by Cardinal Health 200, LLC, United States
FDA product code KMF
Device type Bandage, Liquid
Device class Class 1
Regulation 21 CFR 880.5090
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2026-06-09
Record revised 2024-05-08 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Over the counter Yes
Latex Labelled latex-free
Label carries lot or batch number, expiry date
Packaging Case of 5, carton of 10, case of 10, box of 5, case of 4, box of 10
Sizes Length 2.5 to 91.4 cm; width 5.1 to 30.5 cm

Catalogue Numbers

Catalogue numbers for Kendall
Catalogue number Size Status
9236 Length 10.2 cm In distribution
9232 Length 5.1 cm In distribution
9351 In distribution
9244 Length 91.4 cm In distribution
9356 In distribution
9239 Length 25.4 cm In distribution
9240 Width 10.2 cm In distribution
9231 Length 30.5 cm In distribution
9238 Width 10.2 cm In distribution
9355 In distribution
9243 Length 61 cm In distribution
9242 Width 30.5 cm In distribution
9233 Length 10.2 cm In distribution
9235 Width 5.1 cm In distribution
9354 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
PolyMem Ferris MFG. Corp. 60
3M™ Cavilon™ 3M Company 54
Kendall Cardinal Health 23
Curity Cardinal Health 11
GluSeal® Glustich Inc 7
Stratis Covidien LP 7
Curity Cardinal Health 200, LLC 6
Tritis Covidien LP 4
GluSeal®90 Glustich Inc 3
Medline Medline Industries, Inc. 3
GluSeal®90 Skinstitch Corp. 2
Medline Industries, Inc. Medline Industries, Inc. 2

Showing 12 of 29. All products under Bandage, Liquid

Recalls

1 of these is 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
2020-01-15 Class II Under Investigation by firm Non-sterile product was shipped to customers. Product package is labeled as both “STERILE” and “NON-STERILR” ; the product did not undergo sterilization process and is non-sterile. The usage of a needle that is not sterile could result in 8400 each 2020-12-04

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