510(k) · Cleared
ClearedBand-Aid (R) Brand Liquid Bandage
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Johnson & Johnson Consumer Companies, Inc. · KMF Bandage, Liquid
Cleared on Dec 11, 2006 as substantially equivalent to K022645 (Beiersdorf AG, 2002) and 1 other predicate after a 101-day review. Its family tree reaches back 2 generations to 2001. 1 later device descends from it.
- Decided
- Dec 11, 2006
- Review
- 101 days
- Class
- Class I
- Product code
- KMF
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K002338 (2001). 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
- 1 generation backK022645 CURADBeiersdorf AG · 2002
- This deviceK062602 Band-Aid (R) Brand Liquid BandageJohnson & Johnson Consumer Companies, Inc. · 2006
- Descendant · cites it directly · 0 of its ownK073663 Gelspray Wound DressingBiocure, Inc. · 2008
Most influential descendants
Showing 1 of 1 · See all- K073663Gelspray Wound DressingBiocure, Inc. · 2008 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K002338 | Liquiderm Liquid Adhesive Bandage | Closure Medical Corp. | 2001 | — |
| −1 | K022645 | CURAD | Beiersdorf AG | 2002 | — |
| 0 (this device) | K062602 | Band-Aid (R) Brand Liquid Bandage | Johnson & Johnson Consumer Companies, Inc. | 2006 | — |
| +1 | K073663 | Gelspray Wound Dressing | Biocure, Inc. | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
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 K241916 TearRepair Liquid Skin Protectantscore 8.1 · 1 generation · no Class I recall
What was it cleared against? (2)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K022645 | CURADSummary page 1…Regulatory Class: Class I Product Code: KMF Marketed Device(s) to which Equivalency is Claimed: CURAD® Spray Bandage, K022645 Johnson and Johnson LIQUIDERM Tm BAND- AID® Brand Liqui… | 2002 |
| * | K002338 | Liquiderm Liquid Adhesive BandageSummary page 1…CURAD® Spray Bandage, K022645 Johnson and Johnson LIQUIDERM Tm BAND- AID® Brand Liquid Bandage, K002338 Description of Device: Solvent based liquid bandages are single- use liquid b… | 2001 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K073663 | Gelspray Wound Dressing | 2008 | 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?
- The line of descent spans 5 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K073663 (Biocure, Inc., 2008) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K022645.
How does its category compare?
All KMF devicesKMF Bandage, Liquid: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KMF
1in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · KMF
213in 2009
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KMF
1in 2011
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KMF
12in 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 | — |
What is it indicated for?
The intended use of the BAND-AID® brand solvent based Liquid bandage is for providing a covering over minor cuts and scrapes that are clean and dry
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K062602 · printed Nov 6, 2026
Cite this page
510(k) Report. “K062602: Band-Aid (R) Brand Liquid Bandage.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062602
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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