3m™ Nexcare™

Nexcare™ Liquid Bandage Spray LBS118-03

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
6510(k) clearances naming this product code

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 3M™ Nexcare™
Listed by 3M Company, United States
FDA product code KMF
Device type Bandage, Liquid
Device class Class 1
Regulation 21 CFR 880.5090
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2018-09-25
Record revised 2026-03-30 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Over the counter Yes
Latex Labelled latex-free
Packaging Box of 4

Catalogue Numbers

Catalogue numbers for 3M™ Nexcare™
Catalogue number Size Status
LBS118-03 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
Kendall Cardinal Health 200, LLC 15
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

Showing 12 of 29. All products under Bandage, Liquid

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K153571 2016-08-23
K053409 2006-06-19
K031263 2003-10-07
K982893 1998-10-26
K982892 1998-10-26
K940624 1994-05-04

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