510(k) Report

510(k) · Cleared

Cleared

WoundExpress

K211200510(k) TraditionalCleared Sep 3, 2021134-day reviewClass II21 CFR 870.5800

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

Huntleigh Healthcare, Ltd. · JOW Sleeve, Limb, Compressible

Cleared on Sep 3, 2021 as substantially equivalent to K110159 (Medical Compression Systems (Dbn), Ltd., 2011) and 1 other predicate after a 134-day review. Its family tree reaches back 6 generations to 1992.

Decided
Sep 3, 2021
Review
134 days
Class
Class II
Product code
JOW
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K915638 (1992). 24 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2011: 1 other ancestor2006: 2 other ancestors2002: 2 other ancestors2001: 1 other ancestor2000: 2 other ancestors1999: 1 other ancestor1996: 1 other ancestor1995: 3 other ancestors1992: 2 other ancestors2005: 1 other ancestor2003: 1 other ancestor1997: 1 other ancestorReference device: K172103 · Flowtron DVT5 Small Calf Garment · Getinge (Suzhou) Co., Ltd. · 2018K915638 · Talley TM200 Intermttent Compression Unit · Progressive Medical Technology, Inc. · 1992K022340 · Travelair Portable Compression System · Dynamic Air, Inc. · 2003K061125 · Dvtcare CA5 · Doctors Orders · 2006K103187 · Tripleplay-VT Vascular Therapy System · Wildcat Medical, Inc. · 2011K133274 · Vena Pro · Innovamed Health, LLC · 2014K193020 · VenaPro Vascular Therapy System · Innovamed Health, LLC · 20191990199520002005201020152020
  1. Root · 6 generations backK915638 Talley TM200 Intermttent Compression UnitProgressive Medical Technology, Inc. · 1992
  2. 5 generations backK022340 Travelair Portable Compression SystemDynamic Air, Inc. · 2003
  3. 4 generations backK061125 Dvtcare CA5Doctors Orders · 2006
  4. 3 generations backK103187 Tripleplay-VT Vascular Therapy SystemWildcat Medical, Inc. · 2011
  5. 2 generations backK133274 Vena ProInnovamed Health, LLC · 2014
  6. 1 generation backK193020 VenaPro Vascular Therapy SystemInnovamed Health, LLC · 2019
  7. This deviceK211200 WoundExpressHuntleigh Healthcare, Ltd. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K915638Talley TM200 Intermttent Compression UnitProgressive Medical Technology, Inc.1992—
−5K022340Travelair Portable Compression SystemDynamic Air, Inc.2003—
−4K061125Dvtcare CA5Doctors Orders2006—
−3K103187Tripleplay-VT Vascular Therapy SystemWildcat Medical, Inc.2011—
−2K133274Vena ProInnovamed Health, LLC2014—
−1K193020VenaPro Vascular Therapy SystemInnovamed Health, LLC2019—
0 (this device)K211200WoundExpressHuntleigh Healthcare, Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199220
199530
199610
199710
199910
200020
200110
200220
200310
200510
200620
201110
FIG. 1 — Lineage of K211200, 1992–2021Source: 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 JOW? 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 JOW device

  1. #1 K253555 Flexitouch® Plus Advanced Pneumatic…score 14.8 · 11 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
*K110159Activecare SFT
Summary page 5
…Class: II Review Panel: Cardiovascular 5.2 Predicate Device Information Predicate Devices: ActiveCare+SFT System (K110159) manufactured by Medical Compression Systems (DBN) Ltd. VenaP…
Medical Compression Systems (Dbn), Ltd.2011—
*K193020VenaPro Vascular Therapy System
Summary page 5
…tem (K110159) manufactured by Medical Compression Systems (DBN) Ltd. VenaPro Vascular Therapy System (K193020) manufactured by Innovamed Health, LLC. Regulation Name: Compressible Limb Sle…
Innovamed Health, LLC2019—
†K172103Flowtron DVT5 Small Calf GarmentGetinge (Suzhou) Co., Ltd.2018—

Also cleared against K110159: 1 other device →

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 29 years and passes through 6 companies; a new generation was cleared every 4.7 years on median.
  • 3 of the 24 ancestors have a recall of any class.
  • 1 other device also cites its predicate K110159.

How does its category compare?

All JOW devices

JOW Sleeve, Limb, Compressible: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · JOW

7in 2025

2007: 62008: 42009: 32010: 182011: 112012: 132013: 172014: 162015: 102016: 92017: 92018: 112019: 112020: 142021: 162022: 72023: 62024: 82025: 72026 (partial year): 6
2007high 18 (2010) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JOW

168in 2025

2007: 66 days median2008: 112 days median2009: 84 days median2010: 71 days median2011: 104 days median2012: 63 days median2013: 94 days median2014: 91 days median2015: 160 days median2016: 121 days median2017: 116 days median2018: 136 days median2019: 88 days median2020: 158 days median2021: 132 days median2022: 80 days median2023: 160 days median2024: 197 days median2025: 168 days median2026 (partial year): 252 days median
2007high 252 (2026) · low 63 (2012)2026

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

Recalls per year · JOW

1in 2019

2008: 72010: 22011: 32012: 22017: 12019: 1
2007high 7 (2008) · low 0 (2007)2026

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

Adverse event reports per year · JOW

24in 2025

2007: 122008: 362009: 452010: 662011: 502012: 1002013: 1692014: 932015: 1372016: 1502017: 1492018: 1142019: 1022020: 502021: 342022: 272023: 572024: 302025: 24
2007high 169 (2013) · low 12 (2007)2025

MAUDE reports naming product code JOW, 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
2007666012
20084112736
2009384045
20101871266
201111104350
201213632100
201317940169
20141691093
2015101600137
201691210150
201791161149
2018111360114
201911881102
202014158050
202116132034
2022780027
20236160057
20248197030
20257168024
202662520—

What is it indicated for?

WoundExpress aids in the treatment of the following clinical conditions:

- Chronic wounds including leg ulcers (venous leg ulcers and mixed aetiology leg ulcers)

- The management of lower limb pain

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. “K211200: WoundExpress.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211200

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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