510(k) Report

510(k) · Cleared

Recalled · Class II · 2026

AQUACEL Ag Surgical SP Dressing

K152926510(k) SpecialCleared Jan 21, 2016108-day reviewClass URecalls 1

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

Convatec Limited · FRO Dressing, Wound, Drug

Cleared on Jan 21, 2016 as substantially equivalent to K091034 (Convatec, 2009) after a 108-day review. Its family tree reaches back 5 generations to 1992. It has been recalled once.

Decided
Jan 21, 2016
Review
108 days
Class
Class U
Product code
FRO
Recalls
1
Predicates
1

Its longest line of descent runs back 5 generations to K914604 (1992). 8 ancestors in all, the oldest K891696 (1989). No later device cites it as a predicate yet.

  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 backK091034 Aquacel AG SurgicalConvatec · 2009
  6. This deviceK152926 AQUACEL Ag Surgical SP DressingConvatec Limited · 2016
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—
−1K091034Aquacel AG SurgicalConvatec2009—
0 (this device)K152926AQUACEL Ag Surgical SP DressingConvatec Limited2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
199410
199810
FIG. 1 — Lineage of K152926, 1992–2016Source: 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
*K091034Aquacel AG Surgical
Summary page 4
…Surgical Cover Dressing Classification Name: Dressing, Wound, Drug Product Code: FRO Device Class: Unclassified 510(k) Substantial Equivalence: K091034 ‐ determined substantially equivalent on December 16, 2009 Device Description: AQUACEL™ Ag Surgical SP dressing i…
Convatec2009—

Also cleared against K091034: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Jun 8, 2026Class IIZ-2677-2026Nonconforming Material/ComponentSurgical dressing manufactured out of specification (greater thickness).

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 24 years and passes through 5 companies; a new generation was cleared every 6.1 years on median.
  • None of the 8 ancestors has a recall.
  • 1 other device also cites its predicate K091034.

How does its category compare?

All FRO devices

FRO Dressing, Wound, Drug: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, 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?

AQUACEL® Ag Surgical SP may be used for the management of wounds healing by primary intent (e.g., traumatic and elective post operative wounds/incisions) and as an effective barrier to bacterial penetration to help reduce infection.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K152926: AQUACEL Ag Surgical SP Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K152926

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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