510(k) · Cleared
ClearedSkinless-Skin, Pink Tint (Condom)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Okamoto USA, Inc. · HIS Condom
Cleared on Nov 5, 1987 after a 112-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.
- Decided
- Nov 5, 1987
- Review
- 112 days
- Class
- Class II
- Product code
- HIS
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK872812 Skinless-Skin, Pink Tint (Condom)Okamoto USA, Inc. · 1987
- Descendant · cites it directly · 3 of its ownK090259 Okamoto Ultra ThinOkamoto USA, Inc. · 2009
- Descendant · 2 generations on · 2 of its ownK192669 Extremely Thin 003, ZERO ZERO THREEOkamoto USA, Inc. · 2020
- Descendant · 3 generations on · 0 of its ownK252622 Male Latex Condom HAOkamoto USA, Inc. · 2026
- Descendant · 3 generations on · 0 of its ownK213921 Microthin Natural Rubber Latex CondomSuretex Limited · 2022
Most influential descendants
Showing 4 of 4 · See all- K090259Okamoto Ultra ThinOkamoto USA, Inc. · 2009 · cites it directly3descendants
- K192669Extremely Thin 003, ZERO ZERO THREEOkamoto USA, Inc. · 2020 · 2 generations on2descendants
- K252622Male Latex Condom HAOkamoto USA, Inc. · 2026 · 3 generations on0descendants
- K213921Microthin Natural Rubber Latex CondomSuretex Limited · 2022 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K872812 | Skinless-Skin, Pink Tint (Condom) | Okamoto USA, Inc. | 1987 | — |
| +1 | K090259 | Okamoto Ultra Thin | Okamoto USA, Inc. | 2009 | — |
| +2 | K192669 | Extremely Thin 003, ZERO ZERO THREE | Okamoto USA, Inc. | 2020 | — |
| +3 | K252622 | Male Latex Condom HA | Okamoto USA, Inc. | 2026 | — |
| +3 | K213921 | Microthin Natural Rubber Latex Condom | Suretex Limited | 2022 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2009 | 1 | 0 |
| 2020 | 1 | 0 |
| 2022 | 1 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), 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 K262108 FAMA Male Latex Condoms – Aqueous Lubricant…score 13.3 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K090259 | Okamoto Ultra Thin | 2009 | 3 |
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?
- Of its descendants, K090259 (Okamoto USA, Inc., 2009) has gone furthest, with 3 descendants of its own.
How does its category compare?
All HIS devicesHIS Condom: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · HIS
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HIS
99in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HIS
1in 2013
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HIS
20in 2025
MAUDE reports naming product code HIS, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 7 | 128 | 1 | 10 |
| 2008 | 3 | 157 | 0 | 11 |
| 2009 | 5 | 241 | 0 | 12 |
| 2010 | 1 | — | 0 | 22 |
| 2011 | 3 | 54 | 0 | 15 |
| 2012 | 7 | 106 | 1 | 10 |
| 2013 | 4 | 208 | 1 | 19 |
| 2014 | 7 | 242 | 0 | 16 |
| 2015 | 3 | 136 | 0 | 8 |
| 2016 | 5 | 115 | 0 | 5 |
| 2017 | 4 | 102 | 0 | 8 |
| 2018 | 2 | — | 0 | 11 |
| 2019 | 1 | — | 0 | 15 |
| 2020 | 4 | 240 | 0 | 12 |
| 2021 | 5 | 233 | 0 | 16 |
| 2022 | 10 | 112 | 0 | 18 |
| 2023 | 2 | — | 0 | 10 |
| 2024 | 0 | — | 0 | 7 |
| 2025 | 5 | 99 | 0 | 20 |
| 2026 | 2 | — | 0 | — |
https://510kreport.com/device/K872812 · printed Nov 5, 2026
Cite this page
510(k) Report. “K872812: Skinless-Skin, Pink Tint (Condom).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K872812
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026