510(k) · Cleared
ClearedProderma Liquid Bandage
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Procurement Technology Systems, LLC · KMF Bandage, Liquid
Cleared on May 2, 2007 as substantially equivalent to K002338 (Closure Medical Corp., 2001) and 2 other predicates after a 194-day review. Its family tree reaches back 3 generations to 2001. 5 later devices descend from it.
- Decided
- May 2, 2007
- Review
- 194 days
- Class
- Class I
- Product code
- KMF
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 3 generations to K002338 (2001). 4 ancestors in all. 5 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
- 2 generations backK031321 Liquishield Liquid Bandage, Model LSB 0001Medlogic Global Limited · 2004
- 1 generation backK050757 Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive…Chemence Medical, Inc. · 2006
- This deviceK063202 Proderma Liquid BandageProcurement Technology Systems, LLC · 2007
- Descendant · cites it directly · 3 of its ownK083913 Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009
- Descendant · 2 generations on · 2 of its ownK131384 Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage…Kericure, Inc. · 2014
- Descendant · 3 generations on · 0 of its ownK182733 Rochal Bioshield Silicone FilmRochal Industries, LLC · 2019
- Descendant · 3 generations on · 0 of its ownK171148 Aleo BME Liquid BandageAleo Bme, Inc. · 2018
- Descendant · cites it directly · 0 of its ownK083752 Gluseal 90, Model GLU9010Glustitch, Inc. · 2009
Most influential descendants
Showing 5 of 5 · See all- K083913Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009 · cites it directly3descendants
- K131384Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid BandageKericure, Inc. · 2014 · 2 generations on2descendants
- K182733Rochal Bioshield Silicone FilmRochal Industries, LLC · 2019 · 3 generations on0descendants
- K171148Aleo BME Liquid BandageAleo Bme, Inc. · 2018 · 3 generations on0descendants
- K083752Gluseal 90, Model GLU9010Glustitch, Inc. · 2009 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K002338 | Liquiderm Liquid Adhesive Bandage | Closure Medical Corp. | 2001 | — |
| −2 | K031321 | Liquishield Liquid Bandage, Model LSB 0001 | Medlogic Global Limited | 2004 | — |
| −1 | K050757 | Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional… | Chemence Medical, Inc. | 2006 | — |
| 0 (this device) | K063202 | Proderma Liquid Bandage | Procurement Technology Systems, LLC | 2007 | — |
| +1 | K083913 | Chesson Labs Liquid Bandage | Chesson Laboratory Associates, Inc. | 2009 | — |
| +2 | K131384 | Kericure Advanced Liquid Bandage, Natural Seal Liquid Bandage, Liquid Bandage | Kericure, Inc. | 2014 | — |
| +3 | K182733 | Rochal Bioshield Silicone Film | Rochal Industries, LLC | 2019 | — |
| +3 | K171148 | Aleo BME Liquid Bandage | Aleo Bme, Inc. | 2018 | — |
| +1 | K083752 | Gluseal 90, Model GLU9010 | Glustitch, Inc. | 2009 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 2 | 0 |
| 2014 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 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? (3)
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 |
|---|---|---|---|
| * | K002338 | Liquiderm Liquid Adhesive BandageSummary page 1…Product Code: KMF Classification: Class I CFR Section: 880.5090 Predicate Devices: LiquiderMTrm Liquid Adhesive Bandage - K(002338 MFG By: Closure Medical Corporation Marketed As: Johnson & Johnson Band-Aidt Liquid Ban… | 2001 |
| * | K031321 | Liquishield Liquid Bandage, Model LSB 0001Summary page 1…MFG By: Closure Medical Corporation Marketed As: Johnson & Johnson Band-Aidt Liquid Bandage LiquiShieldTFm Liquid Bandage - K03 1321 MFG By: Medlogic Global Ltd Marketed As: LiquiShieldTM DERMA+FLEX… | 2004 |
| * | K050757 | Flex-Aid Liquid Gel Bandage and Dermaflex Gel Tissue Adhesive Professional Liquid BandageSummary page 1…uid Bandage - K03 1321 MFG By: Medlogic Global Ltd Marketed As: LiquiShieldTM DERMA+FLEXTm Gel Adhesive -1K050757 MEG By: Chemence Medical Products Marketed As: DERMA+FLEXTM Description: ProDe… | 2006 |
What descends from it? (5)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 6 years and passes through 4 companies; a new generation was cleared every 2.1 years on median.
- None of the 4 ancestors has a recall.
- Of its descendants, K083913 (Chesson Laboratory Associates, Inc., 2009) has gone furthest, with 3 descendants of its own.
- 5 other devices also cite its predicate K002338.
How does its category compare?
All KMF devicesKMF Bandage, Liquid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
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?
ProDerma Liquid Bandage is indicated for over-the-counter (OTC) use to cover minor cuts, scrapes and minor irritations of the skin and help protect them from infection.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K063202 · printed Nov 4, 2026
Cite this page
510(k) Report. “K063202: Proderma Liquid Bandage.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K063202
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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