510(k) Report

510(k) · Cleared

Cleared

Powder Free Latex Examination Glove

K173053510(k) TraditionalCleared Jun 6, 2018251-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

Professional Latex Sdn Bhd · LYY Latex Patient Examination Glove

Cleared on Jun 6, 2018 as substantially equivalent to K161833 (Careglove Global Sdn. Bhd., 2017) after a 251-day review. Its family tree reaches back 2 generations to 2016. 3 later devices descend from it.

Decided
Jun 6, 2018
Review
251 days
Class
Class I
Product code
LYY
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K152593 (2016). 3 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2022: 3 descendants clearedK152593 · Latex Examination Glove Powder Free · Careplus (M) Sdn Bhd · 2016K161833 · Latex Examination Glove Powder Free · Careglove Global Sdn. Bhd. · 2017201620182020202220242026
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants K161833 · Latex Examination Glove Powder Free · Careglove Global Sdn. Bhd. · 2017K152593 · Latex Examination Glove Powder Free · Careplus (M) Sdn Bhd · 20160
  1. Root · 2 generations backK152593 Latex Examination Glove Powder FreeCareplus (M) Sdn Bhd · 2016
  2. 1 generation backK161833 Latex Examination Glove Powder FreeCareglove Global Sdn. Bhd. · 2017
  3. This deviceK173053 Powder Free Latex Examination GloveProfessional Latex Sdn Bhd · 2018
  4. Descendant · cites it directly · 2 of its ownK214017 Examination gloves-Type A (Latex gloves)Jiangxi Kemei Medical Apparatus & Instruments Group Co., Ltd. · 2022
  5. Descendant · 2 generations on · 0 of its ownK222612 Powder-Free Latex examination glovesGuangdong Kingfa Sci. & Tech.Co., Ltd. · 2022
  6. Descendant · 2 generations on · 0 of its ownK222693 Single-use medical latex examination gloves (LG100)Fitone Latex Products Co., Ltd. Guangdong · 2022

Most influential descendants

Showing 3 of 3 · See all
  • K214017Examination gloves-Type A (Latex gloves)Jiangxi Kemei Medical Apparatus & Instruments Group Co., Ltd. · 2022 · cites it directly2descendants
  • K222612Powder-Free Latex examination glovesGuangdong Kingfa Sci. & Tech.Co., Ltd. · 2022 · 2 generations on0descendants
  • K222693Single-use medical latex examination gloves (LG100)Fitone Latex Products Co., Ltd. Guangdong · 2022 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K152593Latex Examination Glove Powder FreeCareplus (M) Sdn Bhd2016—
−1K161833Latex Examination Glove Powder FreeCareglove Global Sdn. Bhd.2017—
0 (this device)K173053Powder Free Latex Examination GloveProfessional Latex Sdn Bhd2018—
+1K214017Examination gloves-Type A (Latex gloves)Jiangxi Kemei Medical Apparatus & Instruments Group Co., Ltd.2022—
+2K222612Powder-Free Latex examination glovesGuangdong Kingfa Sci. & Tech.Co., Ltd.2022—
+2K222693Single-use medical latex examination gloves (LG100)Fitone Latex Products Co., Ltd. Guangdong2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202230
FIG. 1 — Lineage of K173053, 2016–2022Source: 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 LYY? 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 LYY device

  1. #1 K202377 Palm Care Latex Examination Powder Free Glovesscore 12.7 · 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
*K161833Latex Examination Glove Powder Free
Summary page 4
…LYY 3.0 Identification of The Legally Marketed Device Predicate Device Name: LATEX EXAMINATION GLOVES POWDER FREE Predicate 510(K) Number: K161833 Manufacturer’s Name: CAREGLOVE GLOBAL SDN BHD 4.0 Description of Device Powder Free Latex Examination Gloves…
Careglove Global Sdn. Bhd.2017—

Also cleared against K161833: 2 other devices →

What descends from it? (3)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K214017Examination gloves-Type A (Latex gloves)Jiangxi Kemei Medical Apparatus & Instruments Group Co., Ltd.20222

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 2 years and passes through 3 companies; a new generation was cleared every 1.2 years on median.
  • None of the 2 ancestors has a recall.
  • Of its descendants, K214017 (Jiangxi Kemei Medical Apparatus & Instruments Group Co., Ltd., 2022) has gone furthest, with 2 descendants of its own.
  • 2 other devices also cite its predicate K161833.

How does its category compare?

All LYY devices

LYY Latex Patient Examination Glove: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · LYY

1in 2025

2007: 122008: 132009: 72010: 132011: 112012: 112013: 62014: 32015: 32016: 42017: 42018: 22019: 12020: 12021: 82022: 142023: 22024: 12025: 1
2007high 14 (2022) · low 1 (2019)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LYY

150in 2022

2007: 75 days median2008: 151 days median2009: 76 days median2010: 106 days median2011: 127 days median2012: 133 days median2013: 131 days median2014: 156 days median2015: 251 days median2016: 142 days median2017: 230 days median2021: 188 days median2022: 150 days median
2007high 251 (2015) · low 75 (2007)2026

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

Recalls per year · LYY

1in 2020

2011: 12020: 1
2007high 1 (2011) · low 0 (2007)2026

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

Adverse event reports per year · LYY

1in 2025

2007: 112008: 142009: 112010: 102011: 42012: 12013: 22014: 62015: 52016: 72017: 72019: 72020: 12021: 12024: 62025: 1
2007high 14 (2008) · low 0 (2018)2025

MAUDE reports naming product code LYY, 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
20071275011
200813151014
2009776011
201013106010
20111112714
20121113301
2013613102
2014315606
2015325105
2016414207
2017423007
20182—00
20191—07
20201—11
2021818801
20221415000
20232—00
20241—06
20251—01
20260—0—

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 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. “K173053: Powder Free Latex Examination Glove.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173053

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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