510(k) Report

510(k) · Cleared

Cleared

BloodSTOP iX Battle Matrix

K160130510(k) TraditionalCleared Jun 29, 2016161-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 Jun 29, 2016 as substantially equivalent to K072474 (Z-Medica Corporation, 2007) and 1 other predicate after a 161-day review. Its family tree reaches back 6 generations to 2000.

Decided
Jun 29, 2016
Review
161 days
Class
Class U
Product code
QSY
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K002550 (2000). 15 ancestors in all, the oldest K821150 (1982). No later device cites it as a predicate yet.

  1. Root · 6 generations backK002550 RDH BandageMarine Polymer Technologies, Inc. · 2000
  2. 5 generations backK013390 QuickclotOn Site Gas Systems, Inc. · 2002
  3. 4 generations backK051955 Quickclot Acs - Accelerated Clotting SpongeZ-Medica Corporation · 2005
  4. 3 generations backK061767 Quikclot 1ST Response & Quikclot Acs+Z-Medica Corporation · 2006
  5. 2 generations backK070010 Quikclot Sport and Quikclot Sport SilverZ-Medica Corporation · 2007
  6. 1 generation backK072474 Quikclot EXZ-Medica Corporation · 2007 · Recalled
  7. This deviceK160130 BloodSTOP iX Battle MatrixLifescience Plus, Inc. · 2016
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K002550RDH BandageMarine Polymer Technologies, Inc.2000—
−5K013390QuickclotOn Site Gas Systems, Inc.2002—
−4K051955Quickclot Acs - Accelerated Clotting SpongeZ-Medica Corporation2005—
−3K061767Quikclot 1ST Response & Quikclot Acs+Z-Medica Corporation2006—
−2K070010Quikclot Sport and Quikclot Sport SilverZ-Medica Corporation2007—
−1K072474Quikclot EXZ-Medica Corporation20071
0 (this device)K160130BloodSTOP iX Battle MatrixLifescience Plus, Inc.2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199510
199820
199910
200010
200220
200710
FIG. 1 — Lineage of K160130, 2000–2016Source: 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? (2)

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
*K072474Quikclot EX
Summary page 5
…e Matrix Device Common Name: Hemostatic Dressing Classification: Unclassified Classification Name: Dressing Product Code: FRO 3. Predicate Devices: • Primary: K072474 QuikClot eX (also marketed as QuikClot Combat Gauze) • K072681 BloodSTOP iX Hemostatic Gauze 4. Device Description: Bloo…
Z-Medica Corporation20071
*K072681Bloodstop Hemostatic Gauze; IX Hemostatic Gauze
Summary page 5
…ssified Classification Name: Dressing Product Code: FRO 3. Predicate Devices: • Primary: K072474 QuikClot eX (also marketed as QuikClot Combat Gauze) • K072681 BloodSTOP iX Hemostatic Gauze 4. Device Description: BloodSTOP iX Battle Matrix is a biocompatible, non-irritating, woven matri…
Lifescience Plus, Inc.2007—

Also cleared against K072474: 7 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 16 years and passes through 4 companies; a new generation was cleared every 1.4 years on median.
  • 1 of the 15 ancestors has a recall of any class.
  • 7 other devices also cite its predicate K072474.

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. 2016, 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 Battle Matrix is indicated for external temporary control of minor to moderate bleeding of traumatic wounds.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K160130: BloodSTOP iX Battle Matrix.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K160130

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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