510(k) · Cleared
ClearedXenostrip-TV Trichomonas Diagnostic Test Kit; Catalog Numbers S1383.01, S1383.02 & S1383.03
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Hellen Professional Services · JWZ Kit, Screening, Trichomonas
Cleared on Aug 22, 2002 after a 212-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 later device descends from it.
- Decided
- Aug 22, 2002
- Review
- 212 days
- Class
- Class I
- Product code
- JWZ
- Recalls
- None
- Predicates
- 0
1 later device descends from it, 1 citing it directly.
- This deviceK020226 Xenostrip-TV Trichomonas Diagnostic Test Kit; Catalog Numbers…Hellen Professional Services · 2002
- Descendant · cites it directly · 0 of its ownK033864 Genzyme Osom Trichomonas Rapid TestGenzyme Corp. · 2004
Most influential descendants
Showing 1 of 1 · See all- K033864Genzyme Osom Trichomonas Rapid TestGenzyme Corp. · 2004 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K020226 | Xenostrip-TV Trichomonas Diagnostic Test Kit; Catalog Numbers S1383.01… | Hellen Professional Services | 2002 | — |
| +1 | K033864 | Genzyme Osom Trichomonas Rapid Test | Genzyme Corp. | 2004 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in JWZ? 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?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K033864 | Genzyme Osom Trichomonas Rapid Test | 2004 | 0 |
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?
- Of its descendants, K033864 (Genzyme Corp., 2004) has gone furthest, with 0 descendants of its own.
How does its category compare?
All JWZ devicesJWZ Kit, Screening, Trichomonas: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JWZ
FDA has decided no JWZ device since 2007.
Median 510(k) review, days · JWZ
Too few JWZ 510(k)s in any year since 2007 to give a median.
Recalls per year · JWZ
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JWZ
No MAUDE report names JWZ since 2007.
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 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 1 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Xenotope Dlsgnostics Inc. XenOStripM- rv Trichomonas Teat is Intended for the qualitative detectlon of Tfichomonas vagfnalls (L'Trlchomonas'3 antigens from vaginal swabs. Early detection and treatment of trichomonas-related diseases (vaginitls, trtchomoniasis) is useful in the prevention and reduction of disease and dkease symptomotogy.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K020226 · printed Nov 6, 2026
Cite this page
510(k) Report. “K020226: Xenostrip-TV Trichomonas Diagnostic Test Kit; Catalog Numbers S1383.01, S1383.02 & S1383.03.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K020226
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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