510(k) Report

510(k) · Cleared

Cleared

Redermax Antibacterial Wound Matrix

K251582510(k) TraditionalCleared Feb 2, 2026255-day reviewClass U

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Beijing Kreate Medical Co., Ltd. · FRO Dressing, Wound, Drug

Cleared on Feb 2, 2026 as substantially equivalent to K051647 (Organogenesis, Inc., 2005) after a 255-day review. Its family tree reaches back 4 generations to 1997. 1 later device descends from it.

Decided
Feb 2, 2026
Review
255 days
Class
Class U
Product code
FRO
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K970566 (1997). 10 ancestors in all, the oldest K895993 (1990). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 1 other ancestor2002: 1 other ancestor2000: 1 other ancestor1998: 1 other ancestor1997: 1 other ancestor1990: 1 other ancestor2026: 1 descendant clearedK970566 · Arglaes Film Dressing · Maersk Medical, Ltd. · 1997K990810 · Arglaes-AB Antimicrobial Barrier Film Dressing & Island Dressing · Maersk Medical, Ltd. · 1999K024054 · Xylos Xcell Antimicrobial Dressing · Xylos Corporation · 2003K051647 · Fortaderm Antimicrobial Wound Dressing · Organogenesis, Inc. · 20051990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 3 other ancestors4 generations back: 2 other ancestors 1 generation forward: 1 descendant K051647 · Fortaderm Antimicrobial Wound Dressing · Organogenesis, Inc. · 2005K024054 · Xylos Xcell Antimicrobial Dressing · Xylos Corporation · 2003K990810 · Arglaes-AB Antimicrobial Barrier Film Dressing & Island Dressing · Maersk Medical, Ltd. · 1999K970566 · Arglaes Film Dressing · Maersk Medical, Ltd. · 19970
  1. Root · 4 generations backK970566 Arglaes Film DressingMaersk Medical, Ltd. · 1997
  2. 3 generations backK990810 Arglaes-AB Antimicrobial Barrier Film Dressing & Island DressingMaersk Medical, Ltd. · 1999
  3. 2 generations backK024054 Xylos Xcell Antimicrobial DressingXylos Corporation · 2003
  4. 1 generation backK051647 Fortaderm Antimicrobial Wound DressingOrganogenesis, Inc. · 2005
  5. This deviceK251582 Redermax Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd. · 2026
  6. Descendant · cites it directly · 0 of its ownK261646 Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K970566Arglaes Film DressingMaersk Medical, Ltd.1997—
−3K990810Arglaes-AB Antimicrobial Barrier Film Dressing & Island DressingMaersk Medical, Ltd.1999—
−2K024054Xylos Xcell Antimicrobial DressingXylos Corporation2003—
−1K051647Fortaderm Antimicrobial Wound DressingOrganogenesis, Inc.2005—
0 (this device)K251582Redermax Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.2026—
+1K261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199010
199710
199810
200010
200110
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K251582, 1997–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K261023 Microdacyn Wound Irrigation Solutionscore 15.5 · 14 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K051647Fortaderm Antimicrobial Wound Dressing
Summary page 8
…21 CFR 807.92(a)(6) The Redermax™ Antibacterial Wound Matrix was compared with the primary predicate, PuraPly® Antimicrobial Wound Matrix (K051647), to evaluate technological characteristics relevant to safety and performance. Both devices are absorbable wound matrices inten…
Organogenesis, Inc.2005—

Also cleared against K051647: 1 other device →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K261646Redermax® Antibacterial Wound MatrixBeijing Kreate Medical Co., Ltd.20260

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 29 years and passes through 4 companies; a new generation was cleared every 3.5 years on median.
  • 1 of the 10 ancestors has a recall of any class.
  • Of its descendants, K261646 (Beijing Kreate Medical Co., Ltd., 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K051647.

How does its category compare?

All FRO devices

FRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · FRO

11in 2025

2007: 292008: 262009: 312010: 312011: 272012: 242013: 192014: 222015: 282016: 282017: 232018: 202019: 162020: 122021: 82022: 92023: 182024: 242025: 112026 (partial year): 17
2007high 31 (2009) · low 8 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FRO

176in 2025

2007: 187 days median2008: 130 days median2009: 136 days median2010: 146 days median2011: 177 days median2012: 96 days median2013: 194 days median2014: 214 days median2015: 249 days median2016: 222 days median2017: 147 days median2018: 206 days median2019: 270 days median2020: 226 days median2021: 275 days median2022: 332 days median2023: 283 days median2024: 263 days median2025: 176 days median2026 (partial year): 254 days median
2007high 332 (2022) · low 96 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FRO

2in 2024

2007: 42008: 12009: 12011: 42013: 12014: 12015: 22016: 32017: 12019: 12021: 62022: 22023: 2, 2 Class I2024: 22026 (partial year): 2
2007high 6 (2021) · low 0 (2010)2026

Class I (2 since 2007) Class II/III not classified

Adverse event reports per year · FRO

192in 2025

2007: 552008: 302009: 452010: 1222011: 422012: 652013: 1392014: 2692015: 2972016: 1472017: 1492018: 1282019: 1362020: 1392021: 1832022: 1762023: 1982024: 2322025: 192
2007high 297 (2015) · low 30 (2008)2025

MAUDE reports naming product code FRO, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200729187455
200826130130
200931136145
2010311460122
201127177442
20122496065
2013191941139
2014222141269
2015282492297
2016282223147
2017231471149
2018202060128
2019162701136
2020122260139
202182756183
202293322176
2023182832 (2)198
2024242632232
2025111760192
2026172542—

What is it indicated for?

Redermax Antibacterial Wound Matrix is intended for the management of wounds.

Redermax Antibacterial Wound Matrix is indicated for the management of:

Partial and full thickness wounds

Pressure ulcers

Venous ulcers

Diabetic ulcers

Chronic vascular ulcers

Tunneled/undermined wounds

Surgical wounds (donor sites/grafts, post-Mohs' surgery, post-laser surgery, podiatric, wound dehiscence)

Trauma wounds (abrasions, lacerations, second-degree burns, and skin tears)

Draining wounds.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K251582: Redermax Antibacterial Wound Matrix.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K251582

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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