510(k) Report

510(k) · Cleared

Cleared

LUOFUCON Extra Silver Gelling Fiber Dressing, LUOFUCON Silver Antibacterial Gelling Fiber Dressing

K210718510(k) TraditionalCleared Mar 23, 2022378-day reviewClass U

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

Huizhou Foryou Medical Devices Co., Ltd. · FRO Dressing, Wound, Drug

Cleared on Mar 23, 2022 as substantially equivalent to K121275 (Convatec, Inc., 2012) and 1 other predicate after a 378-day review. Its family tree reaches back 5 generations to 1992. 2 later devices descend from it.

Decided
Mar 23, 2022
Review
378 days
Class
Class U
Product code
FRO
Recalls
None
Predicates
2

Its longest line of descent runs back 5 generations to K914604 (1992). 8 ancestors in all. 2 later devices descend from it, 2 citing it directly.

  1. Root · 5 generations backK914604 Mepitel Non-Adherent Silicone DressingMolnlycke Clinical Products AB · 1992
  2. 4 generations backK984371 Mepitel Non Adherent Silicone DressingMolnlycke Health Care, Inc. · 1999
  3. 3 generations backK063271 Aquacel Hydrofiber Dressing and Aquacel AG with Hydrofiber Silver…Convatec, A Division of E.R. Squibb & Sons, LLC · 2007
  4. 2 generations backK080383 Aquacel Hydrofiber Wound Dressing and AG Hydrofiber DressingConvatec, A Division of E.R. Squibb & Sons, LLC · 2008
  5. 1 generation backK121275 Aquacel AG Extra Hydrofiber Dressing with Silver and Strengthening…Convatec, Inc. · 2012
  6. This deviceK210718 LUOFUCON Extra Silver Gelling Fiber Dressing, LUOFUCON Silver…Huizhou Foryou Medical Devices Co., Ltd. · 2022
  7. Descendant · cites it directly · 0 of its ownK240485 LUOFUCON® Extra Silver Gelling Fiber Dressing Plus (Prescription…Huizhou Foryou Medical Devices Co., Ltd. · 2024
  8. Descendant · cites it directly · 0 of its ownK221110 LUOFUCON Silver Gelling Fiber Surgical Dressing, LUOFUCON…Huizhou Foryou Medical Devices Co., Ltd. · 2024

Most influential descendants

Showing 2 of 2 · See all
  • K240485LUOFUCON® Extra Silver Gelling Fiber Dressing Plus (Prescription use),LUOFUCON® Silver…Huizhou Foryou Medical Devices Co., Ltd. · 2024 · cites it directly0descendants
  • K221110LUOFUCON Silver Gelling Fiber Surgical Dressing, LUOFUCON Antibacterial Gelling Fiber…Huizhou Foryou Medical Devices Co., Ltd. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K914604Mepitel Non-Adherent Silicone DressingMolnlycke Clinical Products AB1992—
−4K984371Mepitel Non Adherent Silicone DressingMolnlycke Health Care, Inc.1999—
−3K063271Aquacel Hydrofiber Dressing and Aquacel AG with Hydrofiber Silver Impregnated…Convatec, A Division of E.R. Squibb & Sons, LLC2007—
−2K080383Aquacel Hydrofiber Wound Dressing and AG Hydrofiber DressingConvatec, A Division of E.R. Squibb & Sons, LLC2008—
−1K121275Aquacel AG Extra Hydrofiber Dressing with Silver and Strengthening FiberConvatec, Inc.2012—
0 (this device)K210718LUOFUCON Extra Silver Gelling Fiber Dressing, LUOFUCON Silver Antibacterial…Huizhou Foryou Medical Devices Co., Ltd.2022—
+1K240485LUOFUCON® Extra Silver Gelling Fiber Dressing Plus (Prescription…Huizhou Foryou Medical Devices Co., Ltd.2024—
+1K221110LUOFUCON Silver Gelling Fiber Surgical Dressing, LUOFUCON Antibacterial…Huizhou Foryou Medical Devices Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199810
201910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202420
FIG. 1 — Lineage of K210718, 1992–2024Source: 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
Get a 510(k) Report

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.

TypeNumberDeviceApplicantDecidedRecalls
*K121275Aquacel AG Extra Hydrofiber Dressing with Silver and Strengthening Fiber
Summary page 5
…Name: Dressing, Wound, Drug Regulatory Class: Unclassified Product Code: FRO Review Panel: General & Plastic Surgery 3. Predicate Device 510(k) Number: K121275 Product Name: AquacelTM Ag ExtraTM with HydrofiberTM Dressing with Silver and Strengthening Fiber Manu…
Convatec, Inc.2012—
*K183645Silver High Performance Dressing
Summary page 5
…Product Name: AquacelTM Ag ExtraTM with HydrofiberTM Dressing with Silver and Strengthening Fiber Manufacturer: Convatec Inc. 510(k) Number: K183645 澳 K210718…
Advanced Medical Solutions, Ltd.20191

Also cleared against K121275: 5 other devices →

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K240485LUOFUCON® Extra Silver Gelling Fiber Dressing Plus (Prescription use),LUOFUCON® Silver…Huizhou Foryou Medical Devices Co., Ltd.20240
K221110LUOFUCON Silver Gelling Fiber Surgical Dressing, LUOFUCON Antibacterial Gelling Fiber…Huizhou Foryou Medical Devices Co., Ltd.20240

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 30 years and passes through 5 companies; a new generation was cleared every 6.9 years on median.
  • 1 of the 8 ancestors has a recall of any class.
  • Of its descendants, K240485 (Huizhou Foryou Medical Devices Co., Ltd., 2024) has gone furthest, with 0 descendants of its own.
  • 5 other devices also cite its predicate K121275.

How does its category compare?

All FRO devices

FRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, 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?

Prescription:

LUOFUCON® Extra Silver Gelling Fiber Dressing may be used for the management of moderate to heavily exuding chronic and acute wounds as an effective barrier to bacterial penetration of the dressing, including:

Partial thickness burns (second degree);

Diabetic foot ulcers;

Leg ulcers (venous stasis ulcers, arterial ulcers and leg ulcers of mixed etiology);

Pressure ulcers (partial and full thickness);

Donor sites;

Surgical wounds;

Traumatic wounds.

OTC:

LUOFUCON® Silver Antibacterial Gelling Fiber Dressing may be used for:

Minor abrasions;

Minor lacerations;

Minor cuts;

Minor scalds and burns.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K210718: LUOFUCON Extra Silver Gelling Fiber Dressing, LUOFUCON Silver Antibacterial Gelling Fiber Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K210718

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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