510(k) Report

510(k) · Cleared

Cleared

Powdered Synthetic (Yellow) Vinyl Patient Examination Gloves

K011883510(k) TraditionalCleared Jul 17, 200129-day reviewClass I21 CFR 880.6250

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

Shijiazhuang Eversharp Plastic Products Co., Ltd. · LYZ Vinyl Patient Examination Glove

Cleared on Jul 17, 2001 as substantially equivalent to K992862 (Shijiazhuang Great Vision Plastic Products Co., LT, 1999) after a 29-day review. Its family tree reaches back 5 generations to 1989.

Decided
Jul 17, 2001
Review
29 days
Class
Class I
Product code
LYZ
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K893822 (1989). 6 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK893822 Honyee Vinyl Examination GlovesHonyee Enterprise Co. · 1989
  2. 4 generations backK960746 Sunmax Enterprise Shanghai Vinyl Powdered Patient Exam. GlovesSunmax Enterprise Shanghai Co., Ltd. · 1996
  3. 3 generations backK974151 Vinyl Patient Examination Gloves (Powdered)Shanghai Super Gloves Co., Ltd. · 1997
  4. 2 generations backK983645 Synthetic Powdered Vinyl Patient Examination GlovesShijiazhuang Great Eagle Plastic Products Co., Ltd. · 1998
  5. 1 generation backK992862 Synthetic Powdered (Yellow) Vinyl Patient Examination GlovesShijiazhuang Great Vision Plastic Products Co., LT · 1999
  6. This deviceK011883 Powdered Synthetic (Yellow) Vinyl Patient Examination GlovesShijiazhuang Eversharp Plastic Products Co., Ltd. · 2001
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K893822Honyee Vinyl Examination GlovesHonyee Enterprise Co.1989—
−4K960746Sunmax Enterprise Shanghai Vinyl Powdered Patient Exam. GlovesSunmax Enterprise Shanghai Co., Ltd.1996—
−3K974151Vinyl Patient Examination Gloves (Powdered)Shanghai Super Gloves Co., Ltd.1997—
−2K983645Synthetic Powdered Vinyl Patient Examination GlovesShijiazhuang Great Eagle Plastic Products Co., Ltd.1998—
−1K992862Synthetic Powdered (Yellow) Vinyl Patient Examination GlovesShijiazhuang Great Vision Plastic Products Co., LT1999—
0 (this device)K011883Powdered Synthetic (Yellow) Vinyl Patient Examination GlovesShijiazhuang Eversharp Plastic Products Co., Ltd.2001—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
FIG. 1 — Lineage of K011883, 1989–2001Source: 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 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. #1 K260860 Powder Free Synthetic Vinyl Exam Gloves (Blue…score 11.4 · 2 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K992862Synthetic Powdered (Yellow) Vinyl Patient Examination Gloves
Summary page 1
…ent Examination Gloves Predicate Device Information: Shijiazhuang Great Eagle Plastic Products Co., Ltd. Synthetic Powdered (Yellow) Vinyl Patient Examination Gloves K#992862 Device Description: Classified by FDA’s General and Plastic Surgery Device panel as Class I, 21 CFR 880.6250, Powdered Vinyl Pa…
Shijiazhuang Great Vision Plastic Products Co., LT1999—

Also cleared against K992862: 4 other devices →

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 12 years and passes through 6 companies; a new generation was cleared every 1.5 years on median.
  • None of the 6 ancestors has a recall.
  • 4 other devices also cite its predicate K992862.

How does its category compare?

All LYZ devices

LYZ Vinyl Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LYZ

2in 2025

2007: 362008: 182009: 492010: 722011: 332012: 252013: 82014: 402015: 142016: 112017: 92018: 102019: 42020: 42021: 302022: 102023: 22024: 12025: 22026 (partial year): 1
2007high 72 (2010) · low 1 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LYZ

100in 2022

2007: 47 days median2008: 90 days median2009: 71 days median2010: 66 days median2011: 86 days median2012: 84 days median2013: 193 days median2014: 226 days median2015: 180 days median2016: 145 days median2017: 109 days median2018: 80 days median2019: 162 days median2020: 85 days median2021: 91 days median2022: 100 days median
2007high 226 (2014) · low 47 (2007)2026

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

Recalls per year · LYZ

1in 2016

2009: 12011: 32012: 12016: 1
2007high 3 (2011) · low 0 (2007)2026

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

Adverse event reports per year · LYZ

2in 2025

2007: 42010: 22011: 52012: 52013: 22014: 62015: 12016: 112017: 62019: 32020: 12021: 42022: 12023: 12024: 22025: 2
2007high 11 (2016) · low 0 (2008)2025

MAUDE reports naming product code LYZ, 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
2007364704
2008189000
2009497110
2010726602
2011338635
2012258415
2013819302
20144022606
20151418001
201611145111
2017910906
2018108000
2019416203
202048501
2021309104
20221010001
20232—01
20241—02
20252—02
20261—0—

What is it indicated for?

A patient examination glove is disposable device intended for medical purposes that is worn on the examiner’s hand or finger to prevent contamination between patient and examiner.

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. “K011883: Powdered Synthetic (Yellow) Vinyl Patient Examination Gloves.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K011883

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026