510(k) Report

FDA product code · General and plastic surgery

Hemostatic Wound Dressing With Thrombin Or Other Biologics

QSXClass U510(k) required18 decisions since 20020 recalls

18 FDA decisions since 2002. No recall names this code. The most-cited predicate is K030836, named by 8 later devices.

To temporarily control bleeding and cover external wounds.

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

FIG. A — Illustration, general and plastic surgery panel

Twenty years of QSX at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · QSX

1in 2020

2007: 42008: 12009: 12011: 12020: 1
2007high 4 (2007) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QSX

56in 2007

2007: 56 days median
2007high 56 (2007)2026

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

Recalls per year · QSX

No recall names QSX since 2007.

Adverse event reports per year · QSX

No MAUDE report names QSX since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
200745600
20081—00
20091—00
20100—00
20111—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20201—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — QSX by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in QSX? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report