510(k) Report

510(k) · Cleared

Cleared

Male Latex Condom

K012653510(k) AbbreviatedCleared Sep 21, 200139-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

Qingdao Shuang Die Latex Production Co.,Ltd · HIS Condom

Cleared on Sep 21, 2001 as substantially equivalent to K994095 (Thai Nippon Rubber Industry Co., Ltd., 2000) after a 39-day review. Its family tree reaches back 2 generations to 1995.

Decided
Sep 21, 2001
Review
39 days
Class
Class II
Product code
HIS
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K941258 (1995). No later device cites it as a predicate yet.

  1. Root · 2 generations backK941258 Latex CondomSuretex, Ltd. · 1995 · Recalled
  2. 1 generation backK994095 Latex CondomThai Nippon Rubber Industry Co., Ltd. · 2000
  3. This deviceK012653 Male Latex CondomQingdao Shuang Die Latex Production Co.,Ltd · 2001
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K941258Latex CondomSuretex, Ltd.19951
−1K994095Latex CondomThai Nippon Rubber Industry Co., Ltd.2000—
0 (this device)K012653Male Latex CondomQingdao Shuang Die Latex Production Co.,Ltd2001—
FIG. 1 — Lineage of K012653, 1995–2001Source: 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 510(k) statement (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 13.3 · 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? (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
*K994095Latex Condom
Summary page 1
…Proprietary Name: Various Brand Names Common Name: Latex Condom Classification Name: Condom (21 CFR 884.5300) Predicate Device: Thai Nippon Male Latex Condom 510(k)# K994095 Description of Device: This condom is made of a natural rubber latex, which completely covers the erect penis with a closely fit…
Thai Nippon Rubber Industry Co., Ltd.2000—

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 6 years and passes through 3 companies; a new generation was cleared every 4.1 years on median.
  • 1 of the 2 ancestors has a recall of any class.

How does its category compare?

All HIS devices

HIS Condom: FDA decisions, review times, recalls and adverse event reports over 20 years.

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 Qingdao Shuang condom is used for cofitraception and for prophylactic purposes (to help prevent pregnancy and the transmission of sexually transmitted diseases).

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K012653: Male Latex Condom.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K012653

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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