510(k) · Cleared
ClearedMepilex Transfer AG
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Molnlycke Health Care · FRO Dressing, Wound, Drug
Cleared on Apr 5, 2013 as substantially equivalent to K100029 (Molnlycke Health Care, 2010) after a 108-day review. Its family tree reaches back 2 generations to 2007. 2 later devices descend from it.
- Decided
- Apr 5, 2013
- Review
- 108 days
- Class
- Class U
- Product code
- FRO
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K061554 (2007). 2 later devices descend from it, 1 citing it directly.
- Root · 2 generations backK061554 Mepilex AG Absorbent Silicone-Coated DressingMolnlycke Health Care · 2007
- 1 generation backK100029 Mepilex Border AG DressingMolnlycke Health Care · 2010
- This deviceK123892 Mepilex Transfer AGMolnlycke Health Care · 2013
- Descendant · cites it directly · 1 of its ownK123756 CovagenCovalon Technologies, Ltd. · 2013
- Descendant · 2 generations on · 0 of its ownK192346 scaffolene CL100 Bioresorbable Collagen MatrixFreudenberg Technology Innovation SE & Co. KG · 2020
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K061554 | Mepilex AG Absorbent Silicone-Coated Dressing | Molnlycke Health Care | 2007 | — |
| −1 | K100029 | Mepilex Border AG Dressing | Molnlycke Health Care | 2010 | — |
| 0 (this device) | K123892 | Mepilex Transfer AG | Molnlycke Health Care | 2013 | — |
| +1 | K123756 | Covagen | Covalon Technologies, Ltd. | 2013 | — |
| +2 | K192346 | scaffolene CL100 Bioresorbable Collagen Matrix | Freudenberg Technology Innovation SE & Co. KG | 2020 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2013 | 1 | 0 |
| 2020 | 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 FRO? 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 FRO device
- #1 K261023 Microdacyn Wound Irrigation Solutionscore 15.5 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
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 |
|---|---|---|---|
| * | K100029 | Mepilex Border AG DressingSummary page 2…s required. Conclusion: Based on the information presented in this submission, it can be concluded that the Mepilex@ Transfer Ag is equivalent to the Mepilex® Border Ag (K100029) predicate with respect to intended use, materials, design, and technological characteristics. The only difference in the two mat… | 2010 |
What descends from it? (2)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K123756 | Covagen | 2013 | 1 |
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 1 company; a new generation was cleared every 3.6 years on median.
- None of the 2 ancestors has a recall.
- Of its descendants, K123756 (Covalon Technologies, Ltd., 2013) has gone furthest, with 1 descendant of its own.
- 4 other devices also cite its predicate K100029.
How does its category compare?
All FRO devicesFRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · FRO
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FRO
176in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FRO
2in 2024
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · FRO
192in 2025
MAUDE reports naming product code FRO, 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 | 29 | 187 | 4 | 55 |
| 2008 | 26 | 130 | 1 | 30 |
| 2009 | 31 | 136 | 1 | 45 |
| 2010 | 31 | 146 | 0 | 122 |
| 2011 | 27 | 177 | 4 | 42 |
| 2012 | 24 | 96 | 0 | 65 |
| 2013 | 19 | 194 | 1 | 139 |
| 2014 | 22 | 214 | 1 | 269 |
| 2015 | 28 | 249 | 2 | 297 |
| 2016 | 28 | 222 | 3 | 147 |
| 2017 | 23 | 147 | 1 | 149 |
| 2018 | 20 | 206 | 0 | 128 |
| 2019 | 16 | 270 | 1 | 136 |
| 2020 | 12 | 226 | 0 | 139 |
| 2021 | 8 | 275 | 6 | 183 |
| 2022 | 9 | 332 | 2 | 176 |
| 2023 | 18 | 283 | 2 (2) | 198 |
| 2024 | 24 | 263 | 2 | 232 |
| 2025 | 11 | 176 | 0 | 192 |
| 2026 | 17 | 254 | 2 | — |
What is it indicated for?
Mepilex® Transfer Ag dressing is indicated for the management of a wide range of exuding wounds such as leg and foot ulcers, pressure ulcers, partial thickness burns, traumatic and surgical wounds.
Mepilex® Transfer Ag can also be used under compression bandaging.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K123892 · printed Nov 6, 2026
Cite this page
510(k) Report. “K123892: Mepilex Transfer AG.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K123892
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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