510(k) · Cleared

Cleared

Liquiderm Liquid Adhesive Bandage

K002338510(k) TraditionalCleared Jan 29, 2001181-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

Closure Medical Corp. · KMF Bandage, Liquid

Cleared on Jan 29, 2001 after a 181-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 23 later devices descend from it.

Decided: Jan 29, 2001
Review: 181 days
Class: Class I
Product code: KMF
Recalls: None
Predicates: 0

23 later devices descend from it, 6 citing it directly.

This deviceK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
Descendant · cites it directly · 16 of its ownK022645 CURADBeiersdorf AG · 2002
Descendant · 2 generations on · 8 of its ownK032948 Elastic Skin Liquid BandageMedpak, LLC · 2004
Descendant · 3 generations on · 7 of its ownK042610 DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH · 2005
Descendant · cites it directly · 7 of its ownK031321 Liquishield Liquid Bandage, Model LSB 0001Medlogic Global Limited · 2004
Descendant · 2 generations on · 6 of its ownK050757 Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive…Chemence Medical, Inc. · 2006

Showing 5 of 23 descendants. See all descendants

Descendants cleared per year

2002high 4 (2006) · low 0 (2003)2026

Most influential descendants

Showing 5 of 23 · See all

K022645CURADBeiersdorf AG · 2002 · cites it directly16descendants
K032948Elastic Skin Liquid BandageMedpak, LLC · 2004 · 2 generations on8descendants
K042610DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH · 2005 · 3 generations on7descendants
K031321Liquishield Liquid Bandage, Model LSB 0001Medlogic Global Limited · 2004 · cites it directly7descendants
K050757Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid BandageChemence Medical, Inc. · 2006 · 2 generations on6descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K002338	Liquiderm Liquid Adhesive Bandage	Closure Medical Corp.	2001	—
+1	K022645	CURAD	Beiersdorf AG	2002	—
+2	K032948	Elastic Skin Liquid Bandage	Medpak, LLC	2004	—
+3	K042610	DR. Theiss Alergol Pollen Blocker Cream	Dr. Theiss Naturwaren GmbH	2005	—
+1	K031321	Liquishield Liquid Bandage, Model LSB 0001	Medlogic Global Limited	2004	—
+2	K050757	Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional…	Chemence Medical, Inc.	2006	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2002	1	0
2004	2	0
2005	1	0
2006	4	0
2007	1	0
2008	1	0
2009	3	0
2012	2	0
2013	1	0
2014	2	0
2017	1	0
2018	1	0
2019	1	0
2021	1	0
2022	1	0

FIG. 1 — Lineage of K002338, 2001–2022Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), 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 K241916 TearRepair Liquid Skin Protectantscore 8.1 · 1 generation · no Class I recall

Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (23)

See all 23

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

Number	Device	Applicant	Decided	Descendants
K022645	CURAD	Beiersdorf AG	2002	16
K031321	Liquishield Liquid Bandage, Model LSB 0001	Medlogic Global Limited	2004	7
K063202	Proderma Liquid Bandage	Procurement Technology Systems, LLC	2007	5
K083087	Ecocel	Polichem S.A	2009	1
K062602	Band-Aid (R) Brand Liquid Bandage	Johnson & Johnson Consumer Companies, Inc.	2006	1
K083752	Gluseal 90, Model GLU9010	Glustitch, Inc.	2009	0

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?

Of its descendants, K022645 (Beiersdorf AG, 2002) has gone furthest, with 16 descendants of its own.

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

2007high 3 (2008) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KMF

213in 2009

2007high 213 (2009) · low 35 (2008)2026

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

Recalls per year · KMF

1in 2011

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

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

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	2	—	1	6
2008	3	35	0	2
2009	3	213	0	6
2010	1	—	0	7
2011	0	—	1	16
2012	1	—	0	3
2013	0	—	0	34
2014	2	—	0	24
2015	0	—	0	13
2016	2	—	0	18
2017	0	—	0	16
2018	1	—	0	10
2019	1	—	0	6
2020	0	—	0	8
2021	0	—	0	10
2022	0	—	0	7
2023	0	—	0	6
2024	1	—	0	6
2025	0	—	0	12
2026	0	—	0	—

https://510kreport.com/device/K002338 · printed Nov 6, 2026

Cite this page

510(k) Report. “K002338: Liquiderm Liquid Adhesive Bandage.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K002338

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Record history

FDA decision record loaded May 2, 2026
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026