510(k) Report

510(k) · Cleared

Cleared

Kimberly-Clark Low Barrier, Astm 2100 Face Masks

K110455510(k) AbbreviatedCleared Apr 29, 201173-day reviewClass II21 CFR 878.4040

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

Kimberly-Clark Corp. · FXX Mask, Surgical

Cleared on Apr 29, 2011 as substantially equivalent to K082258 (Crosstex International, 2008) after a 73-day review. Its family tree reaches back 3 generations to 1987. 289 later devices descend from it.

Decided
Apr 29, 2011
Review
73 days
Class
Class II
Product code
FXX
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K874608 (1987). 5 ancestors in all, the oldest K801036 (1980). 289 later devices descend from it, 19 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1980: 1 other ancestor1991: 1 other ancestor2024: 12 descendants cleared2021: 156 descendants cleared2022: 70 descendants cleared2015: 3 descendants cleared2016: 2 descendants cleared2020: 15 descendants cleared2013: 1 descendant cleared2011: 1 descendant cleared2026: 4 descendants cleared2014: 1 descendant cleared2025: 4 descendants cleared2019: 4 descendants cleared2023: 15 descendants cleared2018: 1 descendant clearedK874608 · Tecnol Fluid Shield Surgical Mask · Tecnol New Jersey Wound Care, Inc. · 1987K955556 · Fluid Resistant Mask · American Threshold Healthcare · 1996K082258 · Crosstex Isolite and Isofluid Earloop Face Masks and Isofluid Fogfree Face Masks with and Without Splash Visor · Crosstex International · 200819801990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 19 descendants2 generations forward: 57 descendants3 generations forward: 39 descendants4 generations forward: 54 descendants5 generations forward: 75 descendants6 generations forward: 35 descendants7 generations forward: 7 descendants8 generations forward: 3 descendants K082258 · Crosstex Isolite and Isofluid Earloop Face Masks and Isofluid Fogfree Face Masks with and Without Splash Visor · Crosstex International · 2008K955556 · Fluid Resistant Mask · American Threshold Healthcare · 1996K874608 · Tecnol Fluid Shield Surgical Mask · Tecnol New Jersey Wound Care, Inc. · 19870+5
  1. Root · 3 generations backK874608 Tecnol Fluid Shield Surgical MaskTecnol New Jersey Wound Care, Inc. · 1987
  2. 2 generations backK955556 Fluid Resistant MaskAmerican Threshold Healthcare · 1996
  3. 1 generation backK082258 Crosstex Isolite and Isofluid Earloop Face Masks and Isofluid…Crosstex International · 2008
  4. This deviceK110455 Kimberly-Clark Low Barrier, Astm 2100 Face MasksKimberly-Clark Corp. · 2011
  5. Descendant · cites it directly · 262 of its ownK111402 KC200, Surgical Mask, KC200, Procedure Mask, KC300, Surgicalmask…Kimberly-Clark · 2011
  6. Descendant · cites it directly · 185 of its ownK131879 KC 300 Surgical MaskKimberly-Clark Corp. · 2013 · Recalled
  7. Descendant · 2 generations on · 170 of its ownK133070 SURGICAL FACE MASK (Ear Loops and Tie-on)Bh Medical Products Co., Ltd. · 2015
  8. Descendant · 3 generations on · 158 of its ownK153496 Disposable Surgical Face MaskXiantao Rayxin Medical Products Co., Ltd. · 2016
  9. Descendant · cites it directly · 60 of its ownK160269 Surgical Face Masks (Ear loops and Tie-on)San-M Package Co., Ltd. · 2016

Showing 5 of 289 descendants. See all descendants

Descendants cleared per year

2011: 12013: 12014: 12015: 32016: 22018: 12019: 42020: 152021: 1562022: 702023: 152024: 122025: 42026: 4
2011high 156 (2021) · low 0 (2012)2026

Most influential descendants

Showing 5 of 289 · See all
  • K111402KC200, Surgical Mask, KC200, Procedure Mask, KC300, Surgicalmask, Fluidshield, KC300…Kimberly-Clark · 2011 · cites it directly262descendants
  • K131879KC 300 Surgical MaskKimberly-Clark Corp. · 2013 · cites it directly185descendants
  • K133070SURGICAL FACE MASK (Ear Loops and Tie-on)Bh Medical Products Co., Ltd. · 2015 · 2 generations on170descendants
  • K153496Disposable Surgical Face MaskXiantao Rayxin Medical Products Co., Ltd. · 2016 · 3 generations on158descendants
  • K160269Surgical Face Masks (Ear loops and Tie-on)San-M Package Co., Ltd. · 2016 · cites it directly60descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K874608Tecnol Fluid Shield Surgical MaskTecnol New Jersey Wound Care, Inc.1987—
−2K955556Fluid Resistant MaskAmerican Threshold Healthcare1996—
−1K082258Crosstex Isolite and Isofluid Earloop Face Masks and Isofluid Fogfree Face…Crosstex International2008—
0 (this device)K110455Kimberly-Clark Low Barrier, Astm 2100 Face MasksKimberly-Clark Corp.2011—
+1K111402KC200, Surgical Mask, KC200, Procedure Mask, KC300, Surgicalmask, Fluidshield…Kimberly-Clark2011—
+1K131879KC 300 Surgical MaskKimberly-Clark Corp.20131
+2K133070SURGICAL FACE MASK (Ear Loops and Tie-on)Bh Medical Products Co., Ltd.2015—
+3K153496Disposable Surgical Face MaskXiantao Rayxin Medical Products Co., Ltd.2016—
+1K160269Surgical Face Masks (Ear loops and Tie-on)San-M Package Co., Ltd.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199110

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201110
201310
201410
201530
201620
201810
201940
2020150
20211560
2022700
2023150
2024120
202540
202640
FIG. 1 — Lineage of K110455, 1987–2026Source: 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), 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 FXX? 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 FXX device

  1. #1 K201479 DemeMASKscore 40.2 · 6 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? (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
*K082258Crosstex Isolite and Isofluid Earloop Face Masks and Isofluid Fogfree Face Masks with…
Summary page 2
…gle use, disposable device, provided non-sterile. Comparison to Predicate Devices: Please reference section 11, substantial equivalence. Predicate Device: K082258 Crosstex Isolite, Isofluid, Ultra Fluid Resistant and Procedural Face Masks The following tests were conducted in support…
Crosstex International2008—

Also cleared against K082258: 3 other devices →

What descends from it? (289)

See all 289

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

NumberDeviceApplicantDecidedDescendants
K111402KC200, Surgical Mask, KC200, Procedure Mask, KC300, Surgicalmask, Fluidshield, KC300…Kimberly-Clark2011262
K131879KC 300 Surgical MaskKimberly-Clark Corp.2013185
K160269Surgical Face Masks (Ear loops and Tie-on)San-M Package Co., Ltd.201660
K201729Medical MaskZhende Medical Co., Ltd.20205
K212368Surgical Face MaskAnhui Tiankang Medical Technology Co., Ltd.20214
K232777FLUIDSHIELD* 1 Procedure Mask with SO SOFT* Lining and SO SOFT* Earloops, Lavender…Owens & Minor (O&M) Halyard, Inc.20241
K210150Disposable Medical maskHubei Wanli Protective Products Co., Ltd.20211
K202137Disposable medical maskU-Play Products Corporation20211
K142990Insta-Gard Surgical and Procedure Face MaskCardinal Health200, LLC20151
K232824FLUIDSHIELD* 1 Fog-Free Procedure Mask with SO SOFT* Lining and SO SOFT* Earloops, White…Owens & Minor (O&M) Halyard, Inc.20240

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 24 years and passes through 4 companies; a new generation was cleared every 8.4 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K111402 (Kimberly-Clark, 2011) has gone furthest, with 262 descendants of its own.
  • 3 other devices also cite its predicate K082258.

How does its category compare?

All FXX devices

FXX Mask, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · FXX

6in 2025

2007: 22008: 22009: 12010: 72011: 62012: 12013: 32014: 12015: 52016: 52017: 12018: 32019: 42020: 272021: 2182022: 912023: 222024: 152025: 62026 (partial year): 5
2007high 218 (2021) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FXX

123in 2025

2010: 144 days median2011: 137 days median2013: 219 days median2015: 298 days median2016: 268 days median2018: 119 days median2019: 124 days median2020: 113 days median2021: 162 days median2022: 113 days median2023: 139 days median2024: 263 days median2025: 123 days median2026 (partial year): 142 days median
2007high 298 (2015) · low 113 (2020)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FXX

2in 2024

2019: 22023: 12024: 2
2007high 2 (2019) · low 0 (2007)2026

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

Adverse event reports per year · FXX

11in 2025

2007: 112008: 102009: 32010: 92011: 82012: 222013: 92014: 52015: 142016: 162017: 452018: 212019: 232020: 602021: 672022: 212023: 212024: 212025: 11
2007high 67 (2021) · low 3 (2009)2025

MAUDE reports naming product code FXX, 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
20072—011
20082—010
20091—03
2010714409
2011613708
20121—022
2013321909
20141—05
20155298014
20165268016
20171—045
20183119021
20194124223
202027113060
2021218162067
202291113021
202322139121
202415263221
20256123011
202651420—

What is it indicated for?

The Kimberly-Clark KC100 Face Mask(s) is intended to be worn to protect both the patient and healthcare personnel from transfer of microorganisms, body fluids, and particulate material. These face masks are intended for use in infection control practices to reduce the potential exposure of the wearer to blood and body fluids. The Kimberly-Clark KC100 face mask(s) is a single use, disposable device(s), provided non-sterile.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110455: Kimberly-Clark Low Barrier, Astm 2100 Face Masks.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110455

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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