510(k) Report

510(k) · Cleared

Cleared

Male Latex Condoms

K162919510(k) TraditionalCleared Mar 7, 2017140-day reviewClass II21 CFR 884.5300

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

Zhejiang Xiangban Latex Products Co., Ltd. · HIS Condom

Cleared on Mar 7, 2017 as substantially equivalent to K083817 (Suzhou Colour-Way Enterprise Development Co., Ltd., 2009) after a 140-day review. Its family tree reaches back 3 generations to 1990. 3 later devices descend from it.

Decided
Mar 7, 2017
Review
140 days
Class
Class II
Product code
HIS
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K897129 (1990). 3 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2022: 1 descendant cleared2023: 1 descendant cleared2026: 1 descendant clearedK897129 · Condoms (Multiple Brands) · Sagami, Inc. · 1990K071313 · Trojan-Enz Brand · Church & Dwight Co., Inc. · 2007K083817 · M. Dior Brand · Suzhou Colour-Way Enterprise Development Co., Ltd. · 20091990200020102020
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 2 descendants K083817 · M. Dior Brand · Suzhou Colour-Way Enterprise Development Co., Ltd. · 2009K071313 · Trojan-Enz Brand · Church & Dwight Co., Inc. · 2007K897129 · Condoms (Multiple Brands) · Sagami, Inc. · 19900
  1. Root · 3 generations backK897129 Condoms (Multiple Brands)Sagami, Inc. · 1990
  2. 2 generations backK071313 Trojan-Enz BrandChurch & Dwight Co., Inc. · 2007
  3. 1 generation backK083817 M. Dior BrandSuzhou Colour-Way Enterprise Development Co., Ltd. · 2009
  4. This deviceK162919 Male Latex CondomsZhejiang Xiangban Latex Products Co., Ltd. · 2017
  5. Descendant · cites it directly · 2 of its ownK220576 FAMA Male Latex CondomsShanghai Personage Hygiene Products Co., Ltd. · 2022
  6. Descendant · 2 generations on · 0 of its ownK262108 FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male…Shanghai Personage Hygiene Products Co., Ltd. · 2026
  7. Descendant · 2 generations on · 0 of its ownK232279 LifeStyles NRL Textured CondomSuretex Limited · 2023

Most influential descendants

Showing 3 of 3 · See all
  • K220576FAMA Male Latex CondomsShanghai Personage Hygiene Products Co., Ltd. · 2022 · cites it directly2descendants
  • K262108FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male Latex Condoms –…Shanghai Personage Hygiene Products Co., Ltd. · 2026 · 2 generations on0descendants
  • K232279LifeStyles NRL Textured CondomSuretex Limited · 2023 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K897129Condoms (Multiple Brands)Sagami, Inc.1990—
−2K071313Trojan-Enz BrandChurch & Dwight Co., Inc.2007—
−1K083817M. Dior BrandSuzhou Colour-Way Enterprise Development Co., Ltd.2009—
0 (this device)K162919Male Latex CondomsZhejiang Xiangban Latex Products Co., Ltd.2017—
+1K220576FAMA Male Latex CondomsShanghai Personage Hygiene Products Co., Ltd.2022—
+2K262108FAMA Male Latex Condoms – Aqueous Lubricant (Ultra-thin);FAMA Male Latex…Shanghai Personage Hygiene Products Co., Ltd.2026—
+2K232279LifeStyles NRL Textured CondomSuretex Limited2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
202310
202610
FIG. 1 — Lineage of K162919, 1990–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 HIS? 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 HIS device

  1. #1 K262108 FAMA Male Latex Condoms – Aqueous Lubricant…score 13.2 · 5 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
*K083817M. Dior Brand
Summary page 5
…Page 2 of 4 510(k) Submission The M. Dior Brand male latex condom cleared by FDA through 510(k) No.K083817 (Decision Date – September 16, 2009). The predicate device has not been subject to a design-related recall. 5. Description of t…
Suzhou Colour-Way Enterprise Development Co., Ltd.2009—

Also cleared against K083817: 1 other device →

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K220576FAMA Male Latex CondomsShanghai Personage Hygiene Products 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 27 years and passes through 4 companies; a new generation was cleared every 7.5 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K220576 (Shanghai Personage Hygiene Products Co., Ltd., 2022) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K083817.

How does its category compare?

All HIS devices

HIS Condom: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · HIS

5in 2025

2007: 72008: 32009: 52010: 12011: 32012: 72013: 42014: 72015: 32016: 52017: 42018: 22019: 12020: 42021: 52022: 102023: 22025: 52026 (partial year): 2
2007high 10 (2022) · low 0 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HIS

99in 2025

2007: 128 days median2008: 157 days median2009: 241 days median2011: 54 days median2012: 106 days median2013: 208 days median2014: 242 days median2015: 136 days median2016: 115 days median2017: 102 days median2020: 240 days median2021: 233 days median2022: 112 days median2025: 99 days median
2007high 242 (2014) · low 54 (2011)2026

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

Recalls per year · HIS

1in 2013

2007: 12012: 12013: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · HIS

20in 2025

2007: 102008: 112009: 122010: 222011: 152012: 102013: 192014: 162015: 82016: 52017: 82018: 112019: 152020: 122021: 162022: 182023: 102024: 72025: 20
2007high 22 (2010) · low 5 (2016)2025

MAUDE reports naming product code HIS, 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
20077128110
20083157011
20095241012
20101—022
2011354015
20127106110
20134208119
20147242016
2015313608
2016511505
2017410208
20182—011
20191—015
20204240012
20215233016
202210112018
20232—010
20240—07
2025599020
20262—0—

What is it indicated for?

The Latex Condom for Men is used for contraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted diseases).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K162919: Male Latex Condoms.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K162919

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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