510(k) · Cleared
ClearedVenx Revolution
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Venx, LLC · GAH Stylet, Surgical, General & Plastic Surgery
Cleared on Apr 22, 2011 as substantially equivalent to K000932 (Advanced Medical Products, Inc., 2000) after a 74-day review. Its family tree reaches back 1 generation to 2000.
- Decided
- Apr 22, 2011
- Review
- 74 days
- Class
- Class I
- Product code
- GAH
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K000932 (2000). No later device cites it as a predicate yet.
- Root · 1 generation backK000932 Arachnophlebectomy NeedleAdvanced Medical Products, Inc. · 2000
- This deviceK110355 Venx RevolutionVenx, LLC · 2011
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K000932 | Arachnophlebectomy Needle | Advanced Medical Products, Inc. | 2000 | — |
| 0 (this device) | K110355 | Venx Revolution | Venx, LLC | 2011 | — |
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 GAH? 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
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K000932 | Arachnophlebectomy NeedleSummary page 1…gical Instrument Classification: Class I per 21 CFIR 878.4800 Predicate Device: Advanced Medical Products, Arachnophlebectomy Needle (K000932) Description: The VENX REVOLUTION TM is a sterile, disposable, single patient use surgical instrument for the disruption and dest… | 2000 |
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?
- Its one ancestor has no recall.
How does its category compare?
All GAH devicesGAH Stylet, Surgical, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · GAH
1in 2011
2026 to Oct 25, outlined.
Median 510(k) review, days · GAH
Too few GAH 510(k)s in any year since 2007 to give a median.
Recalls per year · GAH
2in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · GAH
10in 2025
MAUDE reports naming product code GAH, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 2 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 3 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 2 |
| 2022 | 0 | — | 0 | 7 |
| 2023 | 0 | — | 0 | 8 |
| 2024 | 0 | — | 0 | 2 |
| 2025 | 0 | — | 0 | 10 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VENX REVOLUTION TM is a manual surgical instrument intended for use in the destruction of spider veins in the lower extremities of the body.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110355 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110355: Venx Revolution.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110355
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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