510(k) · Cleared
ClearedCURAD
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Beiersdorf AG · KMF Bandage, Liquid
Cleared on Nov 5, 2002 as substantially equivalent to K002338 (Closure Medical Corp., 2001) after an 89-day review. Its family tree reaches back 1 generation to 2001. 16 later devices descend from it.
- Decided
- Nov 5, 2002
- Review
- 89 days
- Class
- Class I
- Product code
- KMF
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K002338 (2001). 16 later devices descend from it, 4 citing it directly.
- Root · 1 generation backK002338 Liquiderm Liquid Adhesive BandageClosure Medical Corp. · 2001
- This deviceK022645 CURADBeiersdorf AG · 2002
- Descendant · cites it directly · 8 of its ownK032948 Elastic Skin Liquid BandageMedpak, LLC · 2004
- Descendant · 2 generations on · 7 of its ownK042610 DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH · 2005
- Descendant · 3 generations on · 6 of its ownK053625 NasalguardTrutek Corp · 2006
- Descendant · 4 generations on · 3 of its ownK132520 Nasal Ease Allergy BlockerHi-Tech Pharmacal, Inc. · 2013
- Descendant · cites it directly · 3 of its ownK083913 Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009
Showing 5 of 16 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 16 · See all- K032948Elastic Skin Liquid BandageMedpak, LLC · 2004 · cites it directly8descendants
- K042610DR. Theiss Alergol Pollen Blocker CreamDr. Theiss Naturwaren GmbH · 2005 · 2 generations on7descendants
- K053625NasalguardTrutek Corp · 2006 · 3 generations on6descendants
- K132520Nasal Ease Allergy BlockerHi-Tech Pharmacal, Inc. · 2013 · 4 generations on3descendants
- K083913Chesson Labs Liquid BandageChesson Laboratory Associates, Inc. · 2009 · cites it directly3descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K002338 | Liquiderm Liquid Adhesive Bandage | Closure Medical Corp. | 2001 | — |
| 0 (this device) | K022645 | CURAD | Beiersdorf AG | 2002 | — |
| +1 | K032948 | Elastic Skin Liquid Bandage | Medpak, LLC | 2004 | — |
| +2 | K042610 | DR. Theiss Alergol Pollen Blocker Cream | Dr. Theiss Naturwaren GmbH | 2005 | — |
| +3 | K053625 | Nasalguard | Trutek Corp | 2006 | — |
| +4 | K132520 | Nasal Ease Allergy Blocker | Hi-Tech Pharmacal, Inc. | 2013 | — |
| +1 | K083913 | Chesson Labs Liquid Bandage | Chesson Laboratory Associates, Inc. | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2006 | 3 | 0 |
| 2008 | 1 | 0 |
| 2009 | 1 | 0 |
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
| 2014 | 2 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 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? (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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K002338 | Liquiderm Liquid Adhesive BandageSummary page 1…iquid bandage KMF 880.5090 General & Plastic Surgery 3. PREDICATE DEVICES LiquidermTMliquid adhesive bandage, 5 lo@) No. K002338. 4. DEVICEDESCRIPTION The product is packaged in a pressurized can. The can is held about 5 inches from affected… | 2001 |
What descends from it? (16)
See all 164 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?
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?
CURAD® Spray Bandage is indicated 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/K022645 · printed Nov 5, 2026
Cite this page
510(k) Report. “K022645: CURAD.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K022645
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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