510(k) Report

510(k) · Cleared

Cleared

Smartwand-DTX

K093557510(k) TraditionalCleared Dec 18, 200932-day reviewClass I21 CFR 880.2740

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

Clearcount Medical Solutions · LWH Counter, Sponge, Surgical

Cleared on Dec 18, 2009 as substantially equivalent to K073180 (Clearcount Medical Solutions, Inc., 2007) and 1 other predicate after a 32-day review. Its family tree reaches back 3 generations to 2006. 1 later device descends from it.

Decided
Dec 18, 2009
Review
32 days
Class
Class I
Product code
LWH
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K060076 (2006). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 1 descendant K073180 · Smartsponge Plus System · Clearcount Medical Solutions, Inc. · 2007K062642 · RF Surgical Systems Inc. Detection System, Model 100A · Rf Surgical Systems, Inc. · 2006K060076 · Surgicount Safety-Sponge System · Surgicount Medical · 2006 · recalled0
  1. Root · 3 generations backK060076 Surgicount Safety-Sponge SystemSurgicount Medical · 2006 · Recalled
  2. 2 generations backK062642 RF Surgical Systems Inc. Detection System, Model 100ARf Surgical Systems, Inc. · 2006
  3. 1 generation backK073180 Smartsponge Plus SystemClearcount Medical Solutions, Inc. · 2007
  4. This deviceK093557 Smartwand-DTXClearcount Medical Solutions · 2009
  5. Descendant · cites it directly · 0 of its ownK113021 Trufreeze System, Trufreeze Spray KitCSA Medical, Inc. · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K113021Trufreeze System, Trufreeze Spray KitCSA Medical, Inc. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K060076Surgicount Safety-Sponge SystemSurgicount Medical20063
−2K062642RF Surgical Systems Inc. Detection System, Model 100ARf Surgical Systems, Inc.2006—
−1K073180Smartsponge Plus SystemClearcount Medical Solutions, Inc.2007—
0 (this device)K093557Smartwand-DTXClearcount Medical Solutions2009—
+1K113021Trufreeze System, Trufreeze Spray KitCSA Medical, Inc.2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K093557, 2006–2012Source: 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 LWH? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin 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
*K073180Smartsponge Plus System
Summary page 1
…Classification Name: Surgical sponge counter, unclassified, 21 CFR 888.2740, LWH Predicate Devices: ClearCount Medical SmartSponge® Plus System K073 180 RE Surgical Systems Detection System K062642 Device Description: The Smart…
Clearcount Medical Solutions, Inc.2007—
*K062642RF Surgical Systems Inc. Detection System, Model 100A
Summary page 1
…LWH Predicate Devices: ClearCount Medical SmartSponge® Plus System K073 180 RE Surgical Systems Detection System K062642 Device Description: The SmartWand-DTXC h System is based on radio frequency…
Rf Surgical Systems, Inc.2006—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K113021Trufreeze System, Trufreeze Spray KitCSA Medical, Inc.20120

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 3 years and passes through 4 companies; a new generation was cleared every 1.0 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K113021 (CSA Medical, Inc., 2012) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LWH devices

LWH Counter, Sponge, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · LWH

2in 2012

2007: 22009: 12010: 12012: 2
2007high 2 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LWH

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

Recalls per year · LWH

1in 2013

2013: 12026 (partial year): 1
2007high 1 (2013) · low 0 (2007)2026

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

Adverse event reports per year · LWH

34in 2025

2007: 12008: 12009: 22010: 32011: 142012: 62013: 52014: 162015: 82016: 402017: 1072018: 642019: 662020: 332021: 352022: 412023: 392024: 372025: 34
2007high 107 (2017) · low 1 (2007)2025

MAUDE reports naming product code LWH, 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—01
20080—01
20091—02
20101—03
20110—014
20122—06
20130—15
20140—016
20150—08
20160—040
20170—0107
20180—064
20190—066
20200—033
20210—035
20220—041
20230—039
20240—037
20250—034
20260—1—

What is it indicated for?

The ClearCount Medical Solutions SmartWand-DTX System is indicated for use in counting and displaying the number of RFID-tagged surgical sponges, laparatomy sponge, and towels detected by the device and providing a non-invasive means of locating retained RFID-tagged surgical sponges, towels, and other tagged items within a surgical site.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K093557: Smartwand-DTX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K093557

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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