510(k) Report

510(k) · Cleared

Cleared

Lifestyles Lubricated Polyisoprene Latex Male Condom

K070800510(k) AbbreviatedCleared Mar 6, 2008349-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

Ansell Healthcare Products, LLC · MOL Condom, Synthetic

Cleared on Mar 6, 2008 as substantially equivalent to K941258 (Suretex, Ltd., 1995) after a 349-day review. Its family tree reaches back 1 generation to 1995. 5 later devices descend from it.

Decided
Mar 6, 2008
Review
349 days
Class
Class II
Product code
MOL
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K941258 (1995). 5 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2016: 1 descendant cleared2024: 1 descendant cleared2023: 1 descendant cleared2017: 1 descendant cleared2018: 1 descendant clearedK941258 · Latex Condom · Suretex, Ltd. · 1995 · recalled1995200020052010201520202025
Descendants, by generation 1 generation forward: 1 descendant2 generations forward: 3 descendants3 generations forward: 1 descendant K941258 · Latex Condom · Suretex, Ltd. · 1995 · recalled0
  1. Root · 1 generation backK941258 Latex CondomSuretex, Ltd. · 1995 · Recalled
  2. This deviceK070800 Lifestyles Lubricated Polyisoprene Latex Male CondomAnsell Healthcare Products, LLC · 2008
  3. Descendant · cites it directly · 4 of its ownK160399 Skyn Original Polyisoprene Lubricated Male CondomAnsell Healthcare Products, LLC · 2016 · Recalled
  4. Descendant · 2 generations on · 1 of its ownK171172 Skyn Original Polyisoprene Lubricated Male Condom - FlavoredAnsell Healthcare Products, LLC · 2017
  5. Descendant · 2 generations on · 0 of its ownK232470 Polyisoprene Extra Large CondomSuretex Limited · 2024
  6. Descendant · 2 generations on · 0 of its ownK231908 45 Micron Polyisoprene CondomSuretex Limited · 2023
  7. Descendant · 3 generations on · 0 of its ownK182438 Synthetic Polyisoprene Lubricated Male Condom - 5 sensesSxwell USA, LLC · 2018

Most influential descendants

Showing 5 of 5 · See all
  • K160399Skyn Original Polyisoprene Lubricated Male CondomAnsell Healthcare Products, LLC · 2016 · cites it directly4descendants
  • K171172Skyn Original Polyisoprene Lubricated Male Condom - FlavoredAnsell Healthcare Products, LLC · 2017 · 2 generations on1descendant
  • K232470Polyisoprene Extra Large CondomSuretex Limited · 2024 · 2 generations on0descendants
  • K23190845 Micron Polyisoprene CondomSuretex Limited · 2023 · 2 generations on0descendants
  • K182438Synthetic Polyisoprene Lubricated Male Condom - 5 sensesSxwell USA, LLC · 2018 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K941258Latex CondomSuretex, Ltd.19951
0 (this device)K070800Lifestyles Lubricated Polyisoprene Latex Male CondomAnsell Healthcare Products, LLC2008—
+1K160399Skyn Original Polyisoprene Lubricated Male CondomAnsell Healthcare Products, LLC20161
+2K171172Skyn Original Polyisoprene Lubricated Male Condom - FlavoredAnsell Healthcare Products, LLC2017—
+2K232470Polyisoprene Extra Large CondomSuretex Limited2024—
+2K23190845 Micron Polyisoprene CondomSuretex Limited2023—
+3K182438Synthetic Polyisoprene Lubricated Male Condom - 5 sensesSxwell USA, LLC2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201710
201810
202310
202410
FIG. 1 — Lineage of K070800, 1995–2024Source: 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 MOL? 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 MOL device

  1. #1 K252158 Sagami Original 002 Polyurethane Male Condomscore 11.4 · 2 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
*K941258Latex Condom
Summary page 1
…Condom (21 CFR 884.5300) Predicate Device: Suretex Ltd., Latex Condoms with Silicone Oil Lubricant 510(k) Document Control Number K941258 Description of the Device: The LifeStyles condom is a male contraceptive and prophylactic device fabricated from…
Suretex, Ltd.19951

Also cleared against K941258: 2 other devices →

What descends from it? (5)

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

NumberDeviceApplicantDecidedDescendants
K160399Skyn Original Polyisoprene Lubricated Male CondomAnsell Healthcare Products, LLC20164

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?

  • Its one ancestor has a recall.
  • Of its descendants, K160399 (Ansell Healthcare Products, LLC, 2016) has gone furthest, with 4 descendants of its own.
  • 2 other devices also cite its predicate K941258.

How does its category compare?

All MOL devices

MOL Condom, Synthetic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · MOL

2in 2025

2008: 22011: 12016: 12017: 22018: 12022: 12023: 12024: 32025: 22026 (partial year): 1
2007high 3 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MOL

244in 2024

2024: 244 days median
2007high 244 (2024)2026

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

Recalls per year · MOL

3in 2018

2018: 3
2007high 3 (2018) · low 0 (2007)2026

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

Adverse event reports per year · MOL

4in 2025

2013: 12014: 32015: 52016: 42017: 92018: 112022: 22023: 22024: 22025: 4
2007high 11 (2018) · low 0 (2007)2025

MAUDE reports naming product code MOL, 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
20070—00
20082—00
20090—00
20100—00
20111—00
20120—00
20130—01
20140—03
20150—05
20161—04
20172—09
20181—311
20190—00
20200—00
20210—00
20221—02
20231—02
2024324402
20252—04
20261—0—

What is it indicated for?

The LifeStyles Lubricated Polyisoprene Latex Male Condom is used for contraception and for prophylactic purposes (to help reduce the risk of pregnancy and the transmission of sexually transmitted diseases, STDs).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K070800: Lifestyles Lubricated Polyisoprene Latex Male Condom.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070800

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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