# K023405: Trojan Mint Tingle Brand Latex Condoms

- Pathway: 510(k) (Abbreviated)
- Applicant: Armkel, LLC
- Decided: Dec 16, 2002 after 67 days
- Product code: HIS (Condom)
- Device class: 2
- Regulation: 21 CFR 884.5300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K890863 (1989). 2 ancestors in all.
6 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013433: Trojan Passion Berry Gel, Armkel, LLC (2002)
- (no number) TROJAN-ENZ Lubricated Condom: named in the summary without a submission number

## Most influential descendants
- K103119: Billy Boy Male Latex Condom (2011), 5 descendants of its own
- K120394: Lifestyles Zero Lubricated Latex Condom (2012), 1 descendant of its own
- K111093: Billy Boy Male Latex Condom (2011), 1 descendant of its own
- K153016: aoni Natural Rubber Latex Condom (2016), 0 descendants of its own
- K141256: Okamoto Studded Condom (2014), 0 descendants of its own

## Indications for use
The TROJAN@MINT TZNGLFM Latex Condom is used for contraception and for prophylactic purposes (to help reduce the risk of pregnancy and the transmission of sexually transmitted diseases; STDs).

Source page: https://510kreport.com/device/K023405
Methodology: https://510kreport.com/methodology