510(k) · Cleared
ClearedPowder Free Vinyl Patient Examination Gloves
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Wealth on (Jiangsu) Co., Ltd. · LYZ Vinyl Patient Examination Glove
Cleared on Apr 19, 2011 as substantially equivalent to K100699 (Shijiazhuang Star Plastic Co., Ltd., 2010) after an 84-day review. Its family tree reaches back 3 generations to 2000. 2 later devices descend from it.
- Decided
- Apr 19, 2011
- Review
- 84 days
- Class
- Class I
- Product code
- LYZ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 3 generations to K000071 (2000). 2 later devices descend from it, 2 citing it directly.
- Root · 3 generations backK000071 Synthetic Powder Free (White) Vinyl Patient Examination GlovesShijiazhuang Great Eagle Plastic Products Co., Ltd. · 2000
- 2 generations backK032908 Fuguan (Brand) Powder-Free Vinyl Patient Examination GlovesShijiazhuang Fuguan Plastic Products Co., Ltd. · 2003
- 1 generation backK100699 Powder-Free Vinyl Patient Examination GlovesShijiazhuang Star Plastic Co., Ltd. · 2010
- This deviceK110219 Powder Free Vinyl Patient Examination GlovesWealth on (Jiangsu) Co., Ltd. · 2011
- Descendant · cites it directly · 0 of its ownK122396 Powered Vinyl Patient Examination Gloves, Clear (Non-Colored)Wealth on (Jiangsu) Co., Ltd. · 2013
- Descendant · cites it directly · 0 of its ownK120584 Power Free Stretch Vinyl Patient Examination GlovesWealth on (Jiangsu) Co., Ltd. · 2012
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K000071 | Synthetic Powder Free (White) Vinyl Patient Examination Gloves | Shijiazhuang Great Eagle Plastic Products Co., Ltd. | 2000 | — |
| −2 | K032908 | Fuguan (Brand) Powder-Free Vinyl Patient Examination Gloves | Shijiazhuang Fuguan Plastic Products Co., Ltd. | 2003 | — |
| −1 | K100699 | Powder-Free Vinyl Patient Examination Gloves | Shijiazhuang Star Plastic Co., Ltd. | 2010 | — |
| 0 (this device) | K110219 | Powder Free Vinyl Patient Examination Gloves | Wealth on (Jiangsu) Co., Ltd. | 2011 | — |
| +1 | K122396 | Powered Vinyl Patient Examination Gloves, Clear (Non-Colored) | Wealth on (Jiangsu) Co., Ltd. | 2013 | — |
| +1 | K120584 | Power Free Stretch Vinyl Patient Examination Gloves | Wealth on (Jiangsu) Co., Ltd. | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
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 LYZ? 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 LYZ device
- #1 K260860 Powder Free Synthetic Vinyl Exam Gloves (Blue…score 11.4 · 2 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin 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 |
|---|---|---|---|
| * | K100699 | Powder-Free Vinyl Patient Examination GlovesSummary page 1…on: I Regulation Number: 21 CFR 880.6250 Panel: General Hospital Product Code: LYZ Predicate Device Information: (1) K100699, "Powder Free Vinyl Patient Examination Gloves, Clear(noncolored)", manufactured by "Shijiazhuang Star Plastic Co., Ltd"… | 2010 |
What descends from it? (2)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
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 11 years and passes through 4 companies; a new generation was cleared every 3.7 years on median.
- None of the 3 ancestors has a recall.
- Of its descendants, K122396 (Wealth on (Jiangsu) Co., Ltd., 2013) has gone furthest, with 0 descendants of its own.
- 6 other devices also cite its predicate K100699.
How does its category compare?
All LYZ devicesLYZ Vinyl Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · LYZ
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LYZ
100in 2022
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LYZ
1in 2016
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LYZ
2in 2025
MAUDE reports naming product code LYZ, 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 | 36 | 47 | 0 | 4 |
| 2008 | 18 | 90 | 0 | 0 |
| 2009 | 49 | 71 | 1 | 0 |
| 2010 | 72 | 66 | 0 | 2 |
| 2011 | 33 | 86 | 3 | 5 |
| 2012 | 25 | 84 | 1 | 5 |
| 2013 | 8 | 193 | 0 | 2 |
| 2014 | 40 | 226 | 0 | 6 |
| 2015 | 14 | 180 | 0 | 1 |
| 2016 | 11 | 145 | 1 | 11 |
| 2017 | 9 | 109 | 0 | 6 |
| 2018 | 10 | 80 | 0 | 0 |
| 2019 | 4 | 162 | 0 | 3 |
| 2020 | 4 | 85 | 0 | 1 |
| 2021 | 30 | 91 | 0 | 4 |
| 2022 | 10 | 100 | 0 | 1 |
| 2023 | 2 | — | 0 | 1 |
| 2024 | 1 | — | 0 | 2 |
| 2025 | 2 | — | 0 | 2 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The powder free vinyl patient examination glove, Clear (non-colored) is a disposable device intended for medical purposes that is worn on the examiner's hand or finger to prevent contamination between patient and examiner. It is sold as non sterile.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K110219 · printed Nov 6, 2026
Cite this page
510(k) Report. “K110219: Powder Free Vinyl Patient Examination Gloves.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K110219
Report an extraction error
Are you the manufacturer?
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