# K143532: Durex Silicone

- Pathway: 510(k) (Traditional)
- Applicant: Reckitt Benckiser, LLC
- Decided: Jul 31, 2015 after 231 days
- Product code: NUC (Lubricant, Personal)
- 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 K062796 (2006). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110690: One Personal Lubricant (Silicone), One (2012) Summary page 4.

## Indications for use
Durex Silicone is indicated for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity and supplement the body’s natural lubrication. This product is compatible with natural rubber latex, polyisoprene, and polyurethane condoms.

Source page: https://510kreport.com/device/K143532
Methodology: https://510kreport.com/methodology