510(k) Report

510(k) · Cleared

Cleared

Exu-Dry Burn/Trauma Dressing, Various Sizes

K864011510(k) TraditionalCleared Nov 22, 198638-day reviewClass I21 CFR 878.4020

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

Fraass Survival Systems, Inc. · NAD Dressing, Wound, Occlusive

Cleared on Nov 22, 1986 after a 38-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Nov 22, 1986
Review
38 days
Class
Class I
Product code
NAD
Recalls
None
Predicates
0

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

Descendants, by year cleared 2009: 1 descendant cleared1990200020102020
  1. This deviceK864011 Exu-Dry Burn/Trauma Dressing, Various SizesFraass Survival Systems, Inc. · 1986
  2. Descendant · cites it directly · 0 of its ownK083659 Silver Wound PadMilliken & Co. · 2009

Most influential descendants

Showing 1 of 1 · See all
  • K083659Silver Wound PadMilliken & Co. · 2009 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K864011Exu-Dry Burn/Trauma Dressing, Various SizesFraass Survival Systems, Inc.1986—
+1K083659Silver Wound PadMilliken & Co.2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
FIG. 1 — Lineage of K864011, 1986–2009Source: 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.

Planning a device in NAD? 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 NAD device

  1. #1 K254246 LT Antibacterial Foam with Silver Dressingscore 13.5 · 6 generations · no Class I recall
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? (1)

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

NumberDeviceApplicantDecidedDescendants
K083659Silver Wound PadMilliken & Co.20090

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, K083659 (Milliken & Co., 2009) has gone furthest, with 0 descendants of its own.

How does its category compare?

All NAD devices

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

FDA decisions per year · NAD

1in 2011

2008: 22009: 12011: 12026 (partial year): 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NAD

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

Recalls per year · NAD

1in 2025

2010: 12014: 12018: 62022: 12025: 1
2007high 6 (2018) · low 0 (2007)2026

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

Adverse event reports per year · NAD

2,619in 2025

2007: 12008: 82009: 92010: 302011: 92012: 32013: 152014: 632015: 2512016: 1062017: 1342018: 1,0292019: 5882020: 5,0352021: 4512022: 4032023: 1,6192024: 1,8042025: 2,619
2007high 5,035 (2020) · low 1 (2007)2025

MAUDE reports naming product code NAD, 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—01
20082—08
20091—09
20100—130
20111—09
20120—03
20130—015
20140—163
20150—0251
20160—0106
20170—0134
20180—61,029
20190—0588
20200—05,035
20210—0451
20220—1403
20230—01,619
20240—01,804
20250—12,619
20261—0—
Cite this page

510(k) Report. “K864011: Exu-Dry Burn/Trauma Dressing, Various Sizes.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K864011

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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