510(k) Report

510(k) · Cleared

Cleared

Curagel Hydrogel Wound Dressing

K950412510(k) TraditionalCleared Mar 24, 199552-day reviewClass I21 CFR 878.4022

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

Kendall Healthcare Products Co. Div.Of Tyco Health · NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic

Cleared on Mar 24, 1995 after a 52-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Mar 24, 1995
Review
52 days
Class
Class I
Product code
NAE
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1996: 1 descendant cleared1995200020052010201520202025
  1. This deviceK950412 Curagel Hydrogel Wound DressingKendall Healthcare Products Co. Div.Of Tyco Health · 1995
  2. Descendant · cites it directly · 0 of its ownK962513 Dermaplex Hydrogel Wound DressingMaxxim Medical · 1996

Most influential descendants

Showing 1 of 1 · See all
  • K962513Dermaplex Hydrogel Wound DressingMaxxim Medical · 1996 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K950412Curagel Hydrogel Wound DressingKendall Healthcare Products Co. Div.Of Tyco Health1995—
+1K962513Dermaplex Hydrogel Wound DressingMaxxim Medical1996—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199610
FIG. 1 — Lineage of K950412, 1995–1996Source: 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.

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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K962513Dermaplex Hydrogel Wound DressingMaxxim Medical19960

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?

  • Of its descendants, K962513 (Maxxim Medical, 1996) has gone furthest, with 0 descendants of its own.

How does its category compare?

All NAE devices

NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · NAE

1in 2009

2008: 22009: 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NAE

Too few NAE 510(k)s in any year since 2007 to give a median.

Recalls per year · NAE

2in 2018

2018: 2
2007high 2 (2018) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · NAE

7in 2025

2012: 12013: 12014: 32015: 172016: 32017: 12018: 42019: 82020: 112021: 152022: 112023: 52024: 132025: 7
2007high 17 (2015) · low 0 (2007)2025

MAUDE reports naming product code NAE, 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
20070—00
20082—00
20091—00
20100—00
20110—00
20120—01
20130—01
20140—03
20150—017
20160—03
20170—01
20180—24
20190—08
20200—011
20210—015
20220—011
20230—05
20240—013
20250—07
20260—0—
Cite this page

510(k) Report. “K950412: Curagel Hydrogel Wound Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K950412

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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