510(k) Report

510(k) · Cleared

Cleared

Romed Latex Surgical Gloves, Powdered, Sterile

K023139510(k) TraditionalCleared Oct 22, 2003397-day reviewClass I21 CFR 878.4460

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

Van Oostveen Medical B.V. · KGO Surgeon'S Gloves

Cleared on Oct 22, 2003 as substantially equivalent to K014278 (Brightway Gloves Pvt., Ltd., 2002) and 1 other predicate after a 397-day review. Its family tree reaches back 1 generation to 2002.

Decided
Oct 22, 2003
Review
397 days
Class
Class I
Product code
KGO
Recalls
None
Predicates
2

Its longest line of descent runs back 1 generation to K021065 (2002). 2 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2002: 1 other ancestorK021065 · Pre-Powdered Sterile Surgeon's Gloves (with a 50 Microgram/GM Protein Claim · Primus Gloves Private, Ltd. · 2002200020022004
Other ancestors, by generation 1 generation back: 1 other ancestor K021065 · Pre-Powdered Sterile Surgeon's Gloves (with a 50 Microgram/GM Protein Claim · Primus Gloves Private, Ltd. · 20020
  1. Root · 1 generation backK021065 Pre-Powdered Sterile Surgeon's Gloves (with a 50 Microgram/GM…Primus Gloves Private, Ltd. · 2002
  2. This deviceK023139 Romed Latex Surgical Gloves, Powdered, SterileVan Oostveen Medical B.V. · 2003
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K021065Pre-Powdered Sterile Surgeon's Gloves (with a 50 Microgram/GM Protein ClaimPrimus Gloves Private, Ltd.2002—
0 (this device)K023139Romed Latex Surgical Gloves, Powdered, SterileVan Oostveen Medical B.V.2003—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
FIG. 1 — Lineage of K023139, 2002–2003Source: 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 KGO? 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 KGO device

  1. #1 K192328 JR.MEDIK Latex Surgeon’s Gloves Powder Freescore 15.2 · 5 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? (2)

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
*K014278Latex Surgeons Glove (Powdered)Brightway Gloves Pvt., Ltd.2002—
*K021065Pre-Powdered Sterile Surgeon's Gloves (with a 50 Microgram/GM Protein ClaimPrimus Gloves Private, Ltd.2002—

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?

  • None of the 2 ancestors has a recall.

How does its category compare?

All KGO devices

KGO Surgeon'S Gloves: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KGO

1in 2025

2007: 102008: 22009: 32010: 62011: 112012: 72013: 62014: 72015: 122016: 92017: 122018: 72019: 112020: 152021: 142022: 62023: 142024: 22025: 12026 (partial year): 2
2007high 15 (2020) · low 1 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGO

185in 2023

2007: 113 days median2009: 48 days median2010: 87 days median2011: 90 days median2012: 133 days median2013: 184 days median2014: 257 days median2015: 225 days median2016: 218 days median2017: 111 days median2018: 194 days median2019: 204 days median2020: 117 days median2021: 199 days median2022: 127 days median2023: 185 days median
2007high 257 (2014) · low 48 (2009)2026

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

Recalls per year · KGO

2in 2023

2009: 152010: 12016: 22017: 12018: 82022: 22023: 2
2007high 15 (2009) · low 0 (2007)2026

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

Adverse event reports per year · KGO

21in 2025

2007: 132008: 82009: 142010: 162011: 142012: 142013: 412014: 282015: 112016: 152017: 202018: 152019: 512020: 152021: 142022: 102023: 282024: 182025: 21
2007high 51 (2019) · low 8 (2008)2025

MAUDE reports naming product code KGO, 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
200710113013
20082—08
20093481514
2010687116
20111190014
20127133014
20136184041
20147257028
201512225011
20169218215
201712111120
20187194815
201911204051
202015117015
202114199014
20226127210
202314185228
20242—018
20251—021
20262—0—

What is it indicated for?

The ROMED surgeon sterile powdered gloves is a single use disposable device made of natural rubber intended to be worn by operating room personnel to protect a surgical wound from contamination.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K023139: Romed Latex Surgical Gloves, Powdered, Sterile.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K023139

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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