510(k) · Cleared
ClearedMedtrade Products Skin Protective Barrier Wipe (Sterile and Preserved)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtrade Products, Ltd. · KMF Bandage, Liquid
Cleared on Nov 8, 2005 as substantially equivalent to K955103 (3M Medical Products Group, 1996) and 1 other predicate after a 195-day review. Its family tree reaches back 2 generations to 1982.
- Decided
- Nov 8, 2005
- Review
- 195 days
- Class
- Class I
- Product code
- KMF
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 2 generations to K821271 (1982). 4 ancestors in all. No later device cites it as a predicate yet.
- Root · 2 generations backK821271 Bard Protective Barrier FilmC.R. Bard, Inc. · 1982
- 1 generation backK973228 Sting Skin Prep Wipe (59420600)/Sting Skin Prep Swab (59420700)Smith & Nephew, Inc. · 1997
- This deviceK051082 Medtrade Products Skin Protective Barrier Wipe (Sterile and Preserved)Medtrade Products, Ltd. · 2005
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K821271 | Bard Protective Barrier Film | C.R. Bard, Inc. | 1982 | — |
| −1 | K973228 | Sting Skin Prep Wipe (59420600)/Sting Skin Prep Swab (59420700) | Smith & Nephew, Inc. | 1997 | — |
| 0 (this device) | K051082 | Medtrade Products Skin Protective Barrier Wipe (Sterile and Preserved) | Medtrade Products, Ltd. | 2005 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1992 | 1 | 0 |
| 1996 | 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 |
|---|---|---|---|
| * | K955103 | 3M NO Sting Barrier FilmSummary page 1…ty assurance level of 10 _6 MedTrade Product Skin Protective Barrier Wipe is technologically the same as the substantially equivalent products, 3M No-Sting Barrier Film K955103 & Smith & Nephew No-sting Skin Prep K<973228. DEPARTMENT OF HEALTH & HUMAN SERVICES… | 1996 |
| * | K973228 | Sting Skin Prep Wipe (59420600)/Sting Skin Prep Swab (59420700)Summary page 1…Skin Protective Barrier Wipe is technologically the same as the substantially equivalent products, 3M No-Sting Barrier Film K955103 & Smith & Nephew No-sting Skin Prep K<973228. DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service… | 1997 |
What descends from it?
No later submission names this one as a predicate yet.
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 23 years and passes through 3 companies; a new generation was cleared every 15.4 years on median.
- None of the 4 ancestors has a recall.
- 4 other devices also cite its predicate K955103.
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?
MedTrade Products Skin Protective Barrier Wipe is a liquid intended for use as a film-forming product, that upon application to intact or damaged skin forms a long lasting waterproof barrier, which acts as a protective interface between the skin and bodily wastes, fluids and adhesive products. It is intended as a primary barrier against irritation from body fluids.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K051082 · printed Nov 4, 2026
Cite this page
510(k) Report. “K051082: Medtrade Products Skin Protective Barrier Wipe (Sterile and Preserved).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K051082
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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