510(k) Report

510(k) · Cleared

Cleared

Non-Adherent Antimicrobial Alginate Dressing, Silvercel Non-Adherent Antimicrobial Alginate Dressing

K081363510(k) TraditionalCleared Sep 24, 2008132-day reviewClass U

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

Advanced Medical Solutions Limited · FRO Dressing, Wound, Drug

Cleared on Sep 24, 2008 as substantially equivalent to K024298 (Advanced Medical Solutions, Ltd., 2003) and 3 other predicates after a 132-day review. Its family tree reaches back 5 generations to 1991.

Decided
Sep 24, 2008
Review
132 days
Class
Class U
Product code
FRO
Recalls
None
Predicates
4

Its longest line of descent runs back 5 generations to K914575 (1991). 10 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK914575 Sorbsan Topical Wound Dressing (Modified)Dow B. Hickam, Inc. · 1991
  2. 4 generations backK983210 Algisite MSmith & Nephew, Inc. · 1998
  3. 3 generations backK002896 Acticoat Foam Dressing, Algisite M Calcium Alginate DressingThe Westaim Corp. · 2001
  4. 2 generations backK041316 Antimicrobial Alginate DressingAdvanced Medical Solutions, Ltd. · 2004
  5. 1 generation backK063173 Modification to Silver Alginate II Wound DressingAdvanced Medical Solutions Limited · 2006
  6. This deviceK081363 Non-Adherent Antimicrobial Alginate Dressing, Silvercel Non-Adherent…Advanced Medical Solutions Limited · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K914575Sorbsan Topical Wound Dressing (Modified)Dow B. Hickam, Inc.1991—
−4K983210Algisite MSmith & Nephew, Inc.1998—
−3K002896Acticoat Foam Dressing, Algisite M Calcium Alginate DressingThe Westaim Corp.2001—
−2K041316Antimicrobial Alginate DressingAdvanced Medical Solutions, Ltd.2004—
−1K063173Modification to Silver Alginate II Wound DressingAdvanced Medical Solutions Limited2006—
0 (this device)K081363Non-Adherent Antimicrobial Alginate Dressing, Silvercel Non-Adherent…Advanced Medical Solutions Limited2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
200010
200210
200310
200710
FIG. 1 — Lineage of K081363, 1991–2008Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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? (4)

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
*K024298Antimicrobial Alginate Dressing
Summary page 1
…l equivalence for the Advanced Medical Solutions Limited's Non-Adherent Antimicrobial Alginate Dressing to the predicate device Antimicrobial Alginate Dressing, 510(k) # K024298, manufactured by Advanced Medical Solutions. The modification to the existing predicate device is the addition of a perforated, n…
Advanced Medical Solutions, Ltd.2003—
*K041316Antimicrobial Alginate Dressing
Summary page 1
…tantial equivalence is claimed:- Antimicrobial Alginate Dressing, 5 10(k) # K024298, manufactured by Advanced Medical Solutions and Silver Alginate II Dressing, 510(k) # K041316/K063173/K070581, manufactured by Advanced Medical Solutions. Device Description:- Non-Adherent Antimicrobial Alginate Dressing i…
Advanced Medical Solutions, Ltd.2004—
*K063173Modification to Silver Alginate II Wound Dressing
Summary page 1
…equivalence is claimed:- Antimicrobial Alginate Dressing, 5 10(k) # K024298, manufactured by Advanced Medical Solutions and Silver Alginate II Dressing, 510(k) # K041316/K063173/K070581, manufactured by Advanced Medical Solutions. Device Description:- Non-Adherent Antimicrobial Alginate Dressing is a ster…
Advanced Medical Solutions Limited2006—
*K070581Silver Alginate II Wound Dressing
Summary page 1
…nce is claimed:- Antimicrobial Alginate Dressing, 5 10(k) # K024298, manufactured by Advanced Medical Solutions and Silver Alginate II Dressing, 510(k) # K041316/K063173/K070581, manufactured by Advanced Medical Solutions. Device Description:- Non-Adherent Antimicrobial Alginate Dressing is a sterile, non…
Advanced Medical Solutions Limited2007—

Also cleared against K024298: 3 other devices →

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 17 years and passes through 5 companies; a new generation was cleared every 2.2 years on median.
  • 1 of the 10 ancestors has a recall of any class.
  • 3 other devices also cite its predicate K024298.

How does its category compare?

All FRO devices

FRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, 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?

Non-Adherent Antimicrobial Alginate Dressing is an effective barrier to bacterial penetration. The barrier functions of the dressing may help reduce infection in moderate to heavily exuding partial and full-thickness wounds, including pressure ulcers, venous ulcers, diabetic ulcers, donor sites, traumatic and surgical wounds.

Non-Adherent Antimicrobial Wound Dressing is indicated for external use only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K081363: Non-Adherent Antimicrobial Alginate Dressing, Silvercel Non-Adherent Antimicrobial Alginate Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K081363

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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