510(k) Report

510(k) · Cleared

Cleared

Powder Free Nitrile Patient Examination Glove, Blue Colored, Non-Sterile, Powder Free Nitrile Patient Examination Glove, White Colored, Non-Sterile

K151750510(k) TraditionalCleared Aug 3, 2016401-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

Kossan International Sdn Bhd · LZA Polymer Patient Examination Glove

Cleared on Aug 3, 2016 as substantially equivalent to K090412 (Gx Corporation Sdn Bhd, 2009) after a 401-day review. Its family tree reaches back 1 generation to 2009. 4 later devices descend from it.

Decided
Aug 3, 2016
Review
401 days
Class
Class I
Product code
LZA
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K090412 (2009). 4 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2018: 1 descendant cleared2016: 1 descendant cleared2017: 2 descendants clearedK090412 · Powder Free Nitrile Examination Gloves (Pink, Green, Orange,White). · Gx Corporation Sdn Bhd · 200920052010201520202025
Descendants, by generation 1 generation forward: 3 descendants2 generations forward: 1 descendant K090412 · Powder Free Nitrile Examination Gloves (Pink, Green, Orange,White). · Gx Corporation Sdn Bhd · 20090
  1. Root · 1 generation backK090412 Powder Free Nitrile Examination Gloves (Pink, Green, Orange,White).Gx Corporation Sdn Bhd · 2009
  2. This deviceK151750 Powder Free Nitrile Patient Examination Glove, Blue Colored…Kossan International Sdn Bhd · 2016
  3. Descendant · cites it directly · 1 of its ownK161215 Brightway Brand Nitrile Examination Gloves, Powder Free…Brightway Holdings Sdn. Bhd. · 2016
  4. Descendant · cites it directly · 0 of its ownK172864 Non-Sterile Powder Free Blue Nitrile Examination Gloves Tested for…Maxter Glove Manufacturing Sdn Bhd · 2018
  5. Descendant · cites it directly · 0 of its ownK171873 Powder Free Nitrile Patient Examination Glove, Blue Colored, Non…Zhonghong Pulin Medical Products Co., Ltd. · 2017
  6. Descendant · 2 generations on · 0 of its ownK171104 Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use…Yty Industry (Manjung) Sdn Bhd · 2017

Most influential descendants

Showing 4 of 4 · See all
  • K161215Brightway Brand Nitrile Examination Gloves, Powder Free, [Sterling/Grey] Tested For Use…Brightway Holdings Sdn. Bhd. · 2016 · cites it directly1descendant
  • K172864Non-Sterile Powder Free Blue Nitrile Examination Gloves Tested for Use with Chemotherapy…Maxter Glove Manufacturing Sdn Bhd · 2018 · cites it directly0descendants
  • K171873Powder Free Nitrile Patient Examination Glove, Blue Colored, Non Sterile, Tested for Use…Zhonghong Pulin Medical Products Co., Ltd. · 2017 · cites it directly0descendants
  • K171104Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use with Chemotherapy…Yty Industry (Manjung) Sdn Bhd · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K090412Powder Free Nitrile Examination Gloves (Pink, Green, Orange,White).Gx Corporation Sdn Bhd2009—
0 (this device)K151750Powder Free Nitrile Patient Examination Glove, Blue Colored, Non-Sterile…Kossan International Sdn Bhd2016—
+1K161215Brightway Brand Nitrile Examination Gloves, Powder Free, [Sterling/Grey]…Brightway Holdings Sdn. Bhd.2016—
+1K172864Non-Sterile Powder Free Blue Nitrile Examination Gloves Tested for Use with…Maxter Glove Manufacturing Sdn Bhd2018—
+1K171873Powder Free Nitrile Patient Examination Glove, Blue Colored, Non Sterile…Zhonghong Pulin Medical Products Co., Ltd.2017—
+2K171104Non-Sterile, Powder Free Nitrile Examination Gloves, Tested for use with…Yty Industry (Manjung) Sdn Bhd2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201720
201810
FIG. 1 — Lineage of K151750, 2009–2018Source: 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 LZA? 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 LZA device

  1. #1 K192333 Blue Nitrile Examination Gloves Powder Freescore 71.0 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K090412Powder Free Nitrile Examination Gloves (Pink, Green, Orange,White).
Summary page 8
…___________________________ K151750 510(k) Summary Page 1 of 14 Predicate Devices: K090412 - Powder Free Nitrile Examination Gloves (Pink, Green, Orange, White). This Product Does Not Contain Thiuram, and/or…
Gx Corporation Sdn Bhd2009—

Also cleared against K090412: 1 other device →

What descends from it? (4)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K161215Brightway Brand Nitrile Examination Gloves, Powder Free, [Sterling/Grey] Tested For Use…Brightway Holdings Sdn. Bhd.20161
K172864Non-Sterile Powder Free Blue Nitrile Examination Gloves Tested for Use with Chemotherapy…Maxter Glove Manufacturing Sdn Bhd20180
K171873Powder Free Nitrile Patient Examination Glove, Blue Colored, Non Sterile, Tested for Use…Zhonghong Pulin Medical Products Co., Ltd.20170

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.
  • Of its descendants, K161215 (Brightway Holdings Sdn. Bhd., 2016) has gone furthest, with 1 descendant of its own.
  • 1 other device also cites its predicate K090412.

How does its category compare?

All LZA devices

LZA Polymer Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · LZA

24in 2025

2007: 212008: 182009: 282010: 312011: 262012: 332013: 202014: 272015: 202016: 302017: 442018: 222019: 252020: 302021: 1392022: 1462023: 622024: 302025: 242026 (partial year): 15
2007high 146 (2022) · low 18 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LZA

110in 2025

2007: 95 days median2008: 97 days median2009: 112 days median2010: 97 days median2011: 122 days median2012: 110 days median2013: 130 days median2014: 197 days median2015: 112 days median2016: 171 days median2017: 124 days median2018: 178 days median2019: 212 days median2020: 101 days median2021: 111 days median2022: 111 days median2023: 92 days median2024: 89 days median2025: 110 days median2026 (partial year): 103 days median
2007high 212 (2019) · low 89 (2024)2026

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

Recalls per year · LZA

3so far in 2026, the most since 2007

2015: 12016: 12026 (partial year): 3
2007high 3 (2026) · low 0 (2007)2026

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

Adverse event reports per year · LZA

73in 2025

2007: 72008: 22009: 122010: 122011: 92012: 112013: 102014: 82015: 122016: 252017: 42018: 32019: 212020: 42021: 202022: 192023: 242024: 762025: 73
2007high 76 (2024) · low 2 (2008)2025

MAUDE reports naming product code LZA, 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
2007219507
2008189702
200928112012
20103197012
20112612209
201233110011
201320130010
20142719708
201520112112
201630171125
20174412404
20182217803
201925212021
20203010104
2021139111020
2022146111019
20236292024
20243089076
202524110073
2026151033—

What is it indicated for?

A patient examination glove is a disposable device intended for medical purposes that is worn on the examiner's hand to prevent contamination between patient and examiner. These gloves were tested for use with chemotherapy drugs as per ASTM D6978-05 (Reapproved 2013) Standard Practice for Assessment of Medical Gloves to Permeation by Chemotherapy Drugs. A patient examination glove is a disposable device intended for medical purposes that is worn on the…

Read the full statement (106 words)

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

These gloves were tested for use with chemotherapy drugs as per ASTM D6978-05 (Reapproved 2013) Standard Practice for Assessment of Medical Gloves to Permeation by Chemotherapy Drugs.

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

These gloves were tested for use with chemotherapy drugs as per ASTM D6978-05 (Reapproved 2013) Standard Practice for Assessment of Medical Gloves to Permeation by Chemotherapy Drugs.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151750: Powder Free Nitrile Patient Examination Glove, Blue Colored, Non-Sterile, Powder Free Nitrile Patient Examination Glove, White Colored, Non-Sterile.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151750

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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