510(k) Report

510(k) · Cleared

Cleared

BloodSTOP iX Trauma Matrix (TM-iX-20)

K253017510(k) TraditionalCleared Apr 30, 2026223-day reviewClass U

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

Lifescience Plus, Inc. · QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics

Cleared on Apr 30, 2026 as substantially equivalent to K123387 (Z-Medica, LLC, 2013) after a 223-day review. Its family tree reaches back 7 generations to 2000.

Decided
Apr 30, 2026
Review
223 days
Class
Class U
Product code
QSY
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K002550 (2000). 16 ancestors in all, the oldest K821150 (1982). No later device cites it as a predicate yet.

  1. Root · 7 generations backK002550 RDH BandageMarine Polymer Technologies, Inc. · 2000
  2. 6 generations backK013390 QuickclotOn Site Gas Systems, Inc. · 2002
  3. 5 generations backK051955 Quickclot Acs - Accelerated Clotting SpongeZ-Medica Corporation · 2005
  4. 4 generations backK061767 Quikclot 1ST Response & Quikclot Acs+Z-Medica Corporation · 2006
  5. 3 generations backK070010 Quikclot Sport and Quikclot Sport SilverZ-Medica Corporation · 2007
  6. 2 generations backK072474 Quikclot EXZ-Medica Corporation · 2007 · Recalled
  7. 1 generation backK123387 Quikclot Hemostatic DressingZ-Medica, LLC · 2013 · Recalled
  8. This deviceK253017 BloodSTOP iX Trauma Matrix (TM-iX-20)Lifescience Plus, Inc. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K002550RDH BandageMarine Polymer Technologies, Inc.2000—
−6K013390QuickclotOn Site Gas Systems, Inc.2002—
−5K051955Quickclot Acs - Accelerated Clotting SpongeZ-Medica Corporation2005—
−4K061767Quikclot 1ST Response & Quikclot Acs+Z-Medica Corporation2006—
−3K070010Quikclot Sport and Quikclot Sport SilverZ-Medica Corporation2007—
−2K072474Quikclot EXZ-Medica Corporation20071
−1K123387Quikclot Hemostatic DressingZ-Medica, LLC20132
0 (this device)K253017BloodSTOP iX Trauma Matrix (TM-iX-20)Lifescience Plus, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199710
199820
200220
200310
200510
200710
FIG. 1 — Lineage of K253017, 2000–2026Source: 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 QSY? 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 QSY device

  1. #1 K240713 Traumagel®score 15.0 · 5 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
*K123387Quikclot Hemostatic Dressing
Summary page 5
…VICE Predicate Manufacturer: Z-Medica, LLC Predicate Trade Name: Quikclot Hemostatic Dressing Predicate 510(k): K123387 Reference Manufacturer: Core Scientific, Ltd. Reference Trade Name: WoundClot Hemostatic Gauze…
Z-Medica, LLC20132
†K140573Woundclot Hemostatic GauzeCore Scientific, Ltd.2014—

Also cleared against K123387: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 26 years and passes through 5 companies; a new generation was cleared every 1.4 years on median.
  • 2 of the 16 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K123387.

How does its category compare?

All QSY devices

QSY Hemostatic Wound Dressing Without Thrombin Or Other Biologics: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · QSY

2in 2025

2007: 132008: 72009: 92010: 72011: 82012: 72013: 32014: 62015: 62016: 52017: 12018: 52019: 42020: 12021: 12022: 22023: 72024: 42025: 22026 (partial year): 2
2007high 13 (2007) · low 1 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QSY

142in 2024

2007: 63 days median2008: 61 days median2009: 55 days median2010: 75 days median2011: 137 days median2012: 239 days median2013: 161 days median2014: 249 days median2015: 171 days median2016: 161 days median2018: 186 days median2019: 336 days median2023: 586 days median2024: 142 days median
2007high 586 (2023) · low 55 (2009)2026

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

Recalls per year · QSY

No recall names QSY since 2007.

Adverse event reports per year · QSY

14in 2025

2022: 12024: 32025: 14
2007high 14 (2025) · low 0 (2007)2025

MAUDE reports naming product code QSY, 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
2007136300
200876100
200995500
201077500
2011813700
2012723900
2013316100
2014624900
2015617100
2016516100
20171—00
2018518600
2019433600
20201—00
20211—00
20222—01
2023758600
2024414203
20252—014
20262—0—

What is it indicated for?

BloodSTOP iX Trauma Matrix is intended for use as a topical dressing for local management of bleeding wounds such as cuts, lacerations and abrasions. It may also be used for external temporary treatment of severely bleeding wounds such as surgical wounds (operative, postoperative, dermatological, etc.) and traumatic injuries.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K253017: BloodSTOP iX Trauma Matrix (TM-iX-20).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K253017

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026