510(k) Report

510(k) · Cleared

Cleared

Carrington Wound Dressing

K902345510(k) TraditionalCleared Jun 7, 199013-day reviewClass U

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

Carrington Laboratories, Inc. · FRO Dressing, Wound, Drug

Cleared on Jun 7, 1990 after a 13-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 of the 67 devices in its family, counting itself, has a Class I recall. 66 later devices descend from it.

Decided
Jun 7, 1990
Review
13 days
Class
Class U
Product code
FRO
Recalls
None
Predicates
0

66 later devices descend from it, 4 citing it directly. 1 of the 67 devices in this family, counting this one, has a Class I recall.

Descendants, by year cleared 1997: 1 descendant cleared1996: 1 descendant cleared2009: 2 descendants cleared1999: 2 descendants cleared2018: 5 descendants cleared2010: 4 descendants cleared2016: 3 descendants cleared2011: 1 descendant cleared2002: 1 descendant cleared2012: 2 descendants cleared, 1 with a Class I recall12014: 6 descendants cleared2024: 5 descendants cleared2015: 7 descendants cleared2013: 3 descendants cleared2025: 4 descendants cleared2019: 2 descendants cleared2017: 3 descendants cleared2026: 9 descendants cleared2023: 2 descendants cleared2020: 1 descendant cleared2022: 2 descendants cleared1990200020102020
  1. This deviceK902345 Carrington Wound DressingCarrington Laboratories, Inc. · 1990
  2. Descendant · cites it directly · 60 of its ownK984413 Bionect HydrogelFidia Pharmaceutical Corp. · 1999
  3. Descendant · 2 generations on · 59 of its ownK020325 L.a.M. Ipm Wound GelL.A.M. Pharmaceutical, Corp. · 2002
  4. Descendant · 3 generations on · 56 of its ownK090725 Oculus Microcyn Wound GelOculus Innovative Sciences, Inc. · 2009
  5. Descendant · 4 generations on · 31 of its ownK100918 Vashe Wound Therapy System Model: 9000-0014Puricore, Inc. · 2010
  6. Descendant · cites it directly · 26 of its ownK090092 Sockit! and Mcmerlin Dermal Wound GelMcmerlin Dental Products LP · 2009

Showing 5 of 66 descendants. See all descendants

Descendants cleared per year

1996: 11997: 11999: 22002: 12009: 22010: 42011: 12012: 22013: 32014: 62015: 72016: 32017: 32018: 52019: 22020: 12022: 22023: 22024: 52025: 42026: 9
1996high 9 (2026) · low 0 (1998)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 66 · See all
  • K984413Bionect HydrogelFidia Pharmaceutical Corp. · 1999 · cites it directly60descendants
  • K020325L.a.M. Ipm Wound GelL.A.M. Pharmaceutical, Corp. · 2002 · 2 generations on59descendants
  • K090725Oculus Microcyn Wound GelOculus Innovative Sciences, Inc. · 2009 · 3 generations on56descendants
  • K100918Vashe Wound Therapy System Model: 9000-0014Puricore, Inc. · 2010 · 4 generations on31descendants
  • K090092Sockit! and Mcmerlin Dermal Wound GelMcmerlin Dental Products LP · 2009 · cites it directly26descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K902345Carrington Wound DressingCarrington Laboratories, Inc.1990—
+1K984413Bionect HydrogelFidia Pharmaceutical Corp.1999—
+2K020325L.a.M. Ipm Wound GelL.A.M. Pharmaceutical, Corp.2002—
+3K090725Oculus Microcyn Wound GelOculus Innovative Sciences, Inc.2009—
+4K100918Vashe Wound Therapy System Model: 9000-0014Puricore, Inc.2010—
+1K090092Sockit! and Mcmerlin Dermal Wound GelMcmerlin Dental Products LP2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199920
200210
200920
201040
201110
201221
201330
201460
201570
201630
201730
201850
201920
202010
202220
202320
202450
202540
202690
FIG. 1 — Lineage of K902345, 1990–2026Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

1 device in this family has a Class I recall. 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (66)

See all 66

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

NumberDeviceApplicantDecidedDescendants
K984413Bionect HydrogelFidia Pharmaceutical Corp.199960
K090092Sockit! and Mcmerlin Dermal Wound GelMcmerlin Dental Products LP200926
K963004Bionect CreamFidia Pharmaceutical Corp.19972
K963228Repliderm Wound DressingOrphan Medical, Inc.19960

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K123113L.a.M. Imp Wound GelGlycobiosciences, Inc. · 2012 · 2 generations on · ◆ in the 2012 descendants bar of FIG. 11 Class I recall

What does this lineage say?

  • Of its descendants, K984413 (Fidia Pharmaceutical Corp., 1999) has gone furthest, with 60 descendants of its own.

How does its category compare?

All FRO devices

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

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—
Cite this page

510(k) Report. “K902345: Carrington Wound Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K902345

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026