510(k) Report

510(k) · Cleared

Cleared

Powerstick Male Latex Condoms

K041717510(k) AbbreviatedCleared Jan 13, 2005203-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

A.P.Deauville, LLC · HIS Condom

Cleared on Jan 13, 2005 as substantially equivalent to K040185 (Ssl Americas, 2004) after a 203-day review. Its family tree reaches back 2 generations to 1990.

Decided
Jan 13, 2005
Review
203 days
Class
Class II
Product code
HIS
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K902509 (1990). 4 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2001: 1 other ancestor1998: 1 other ancestorK902509 · Saxon Ribbed Condoms · Safetex Corp. · 1990K040185 · Durex Studded/Ribbed Lubricated Latex Condom · Ssl Americas · 20041990199520002005
Other ancestors, by generation 2 generations back: 2 other ancestors K040185 · Durex Studded/Ribbed Lubricated Latex Condom · Ssl Americas · 2004K902509 · Saxon Ribbed Condoms · Safetex Corp. · 19900
  1. Root · 2 generations backK902509 Saxon Ribbed CondomsSafetex Corp. · 1990
  2. 1 generation backK040185 Durex Studded/Ribbed Lubricated Latex CondomSsl Americas · 2004
  3. This deviceK041717 Powerstick Male Latex CondomsA.P.Deauville, LLC · 2005
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K902509Saxon Ribbed CondomsSafetex Corp.1990—
−1K040185Durex Studded/Ribbed Lubricated Latex CondomSsl Americas2004—
0 (this device)K041717Powerstick Male Latex CondomsA.P.Deauville, LLC2005—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810
200110
FIG. 1 — Lineage of K041717, 1990–2005Source: 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 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
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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
*K040185Durex Studded/Ribbed Lubricated Latex Condom
Summary page 1
…Name: Condom (21 CFR §884.53 10) Predicate Device: Male Latex Lubricated Condom [5 10(k) Number K0401 85] Descriptiono h Dvc:This condom is made of a natural latex sheath, which completely covers the penis with a closely…
Ssl Americas2004—

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 15 years and passes through 3 companies; a new generation was cleared every 13.8 years on median.
  • None of the 4 ancestors has a recall.

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 Power Stick Male Latex Condom is used for contrceptive 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. “K041717: Powerstick 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/K041717

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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