510(k) Report

510(k) · Cleared

Cleared

Liquishield Liquid Bandage, Model LSB 0001

K031321510(k) TraditionalCleared Jan 21, 2004271-day reviewClass I21 CFR 880.5090

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Medlogic Global Limited · KMF Bandage, Liquid

Cleared on Jan 21, 2004 as substantially equivalent to K002338 (Closure Medical Corp., 2001) after a 271-day review. Its family tree reaches back 1 generation to 2001. 7 later devices descend from it.

Decided
Jan 21, 2004
Review
271 days
Class
Class I
Product code
KMF
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K002338 (2001). 7 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2007: 1 descendant cleared2006: 1 descendant cleared2009: 2 descendants cleared2014: 1 descendant cleared2019: 1 descendant cleared2018: 1 descendant clearedK002338 · Liquiderm Liquid Adhesive Bandage · Closure Medical Corp. · 2001200020052010201520202025
Descendants, by generation 1 generation forward: 2 descendants2 generations forward: 2 descendants3 generations forward: 1 descendant4 generations forward: 2 descendants K002338 · Liquiderm Liquid Adhesive Bandage · Closure Medical Corp. · 20010
  1. Root · 1 generation backK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
  2. This deviceK031321 Liquishield Liquid Bandage, Model LSB 0001Medlogic Global Limited · 2004
  3. Descendant · cites it directly · 6 of its ownK050757 Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive…Chemence Medical, Inc. · 2006
  4. Descendant · cites it directly · 5 of its ownK063202 Proderma Liquid BandageProcurement Technology Systems, LLC · 2007
  5. Descendant · 2 generations on · 3 of its ownK083913 Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009
  6. Descendant · 3 generations on · 2 of its ownK131384 Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage…Kericure, Inc. · 2014
  7. Descendant · 4 generations on · 0 of its ownK182733 Rochal Bioshield Silicone FilmRochal Industries, LLC · 2019

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2006: 12007: 12009: 22014: 12018: 12019: 1
2006high 2 (2009) · low 0 (2008)2026

Most influential descendants

Showing 5 of 7 · See all
  • K050757Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid BandageChemence Medical, Inc. · 2006 · cites it directly6descendants
  • K063202Proderma Liquid BandageProcurement Technology Systems, LLC · 2007 · cites it directly5descendants
  • K083913Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009 · 2 generations on3descendants
  • K131384Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid BandageKericure, Inc. · 2014 · 3 generations on2descendants
  • K182733Rochal Bioshield Silicone FilmRochal Industries, LLC · 2019 · 4 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K002338Liquiderm Liquid Adhesive BandageClosure Medical Corp.2001—
0 (this device)K031321Liquishield Liquid Bandage, Model LSB 0001Medlogic Global Limited2004—
+1K050757Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional…Chemence Medical, Inc.2006—
+1K063202Proderma Liquid BandageProcurement Technology Systems, LLC2007—
+2K083913Chesson Labs Liquid BandageChesson Laboratory Associates, Inc.2009—
+3K131384Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid BandageKericure, Inc.2014—
+4K182733Rochal Bioshield Silicone FilmRochal Industries, LLC2019—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200710
200920
201410
201810
201910
FIG. 1 — Lineage of K031321, 2001–2019Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KMF? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new KMF device

  1. #1 K241916 TearRepair Liquid Skin Protectantscore 8.1 · 1 generation · no Class I recall
Get a 510(k) Report

What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K002338Liquiderm Liquid Adhesive Bandage
Summary page 1
…device: LIQUIDERM TM Liquid Adhesive Bandage manufactured by Closure Medical Corp., K002338, (Marketed as Johnson & Johnson Band-Aid® Liquid Bandage). Intended use:…
Closure Medical Corp.2001—

Also cleared against K002338: 5 other devices →

What descends from it? (7)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K050757Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid BandageChemence Medical, Inc.20066
K063202Proderma Liquid BandageProcurement Technology Systems, LLC20075

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Its one ancestor has no recall.
  • Of its descendants, K050757 (Chemence Medical, Inc., 2006) has gone furthest, with 6 descendants of its own.
  • 5 other devices also cite its predicate K002338.

How does its category compare?

All KMF devices

KMF Bandage, Liquid: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KMF

1in 2024

2007: 22008: 32009: 32010: 12012: 12014: 22016: 22018: 12019: 12024: 1
2007high 3 (2008) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KMF

213in 2009

2008: 35 days median2009: 213 days median
2007high 213 (2009) · low 35 (2008)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · KMF

1in 2011

2007: 12011: 1
2007high 1 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · KMF

12in 2025

2007: 62008: 22009: 62010: 72011: 162012: 32013: 342014: 242015: 132016: 182017: 162018: 102019: 62020: 82021: 102022: 72023: 62024: 62025: 12
2007high 34 (2013) · low 2 (2008)2025

MAUDE reports naming product code KMF, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—16
200833502
2009321306
20101—07
20110—116
20121—03
20130—034
20142—024
20150—013
20162—018
20170—016
20181—010
20191—06
20200—08
20210—010
20220—07
20230—06
20241—06
20250—012
20260—0—

What is it indicated for?

LiquiShield MT Liquid Bandage is intended to cover minor cuts and scrapes and minor irritations of the skin and help protect them from infection.

Indications for use as stated in the FDA summary.

Also cleared against K002338

5 other devices cite the same predicate.

  • K083087EcocelPolichem S.A · 2009
  • K083752Gluseal 90, Model GLU9010Glustitch, Inc. · 2009
  • K063202Proderma Liquid BandageProcurement Technology Systems, LLC · 2007
  • K062602Band-Aid (R) Brand Liquid BandageJohnson & Johnson Consumer Companies, Inc. · 2006
  • K022645CURADBeiersdorf AG · 2002

More from Medlogic Global Limited

5 FDA decisions under this applicant name. See the company

  • K110184Liquiband Flow ControlMedlogic Global Limited · 2011
  • K102076Liquiband Dual, Model LBD 001Medlogic Global Limited · 2011
  • K100284Liquiband Ultima, Lut 003Medlogic Global Limited · 2010
  • K023163Liquishield-S (0.7G), Model LS 0010, Liquishield-S (2.0G), Model LS 0020Medlogic Global Limited · 2003

Recent decisions in KMF

The KMF category page

  • K241916TearRepair Liquid Skin ProtectantOptmed, Inc. · 2024
  • K182733Rochal Bioshield Silicone FilmRochal Industries, LLC · 2019
  • K171148Aleo BME Liquid BandageAleo Bme, Inc. · 2018
  • K153571Cavilon Advanced High Endurance Skin Protectant3M Healthcare · 2016
  • K160684Atteris No-Sting Skin ProtectantRochal Industries, LLC · 2016

https://510kreport.com/device/K031321 · printed Nov 6, 2026

Cite this page

510(k) Report. “K031321: Liquishield Liquid Bandage, Model LSB 0001.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K031321

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026