# K133336: Pjur (R) Siliconegel, Pjur (R) Basic Personal Glide, Pjur (R) Light, Pjur (R) Med Premium Glide

- Pathway: 510(k) (Traditional)
- Applicant: Pjur Group Luxembourg S.A.
- Decided: Jul 24, 2014 after 268 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: 3 generations back to K062796 (2006). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040428: Multiple Erozone Bodyglide Fluid, Erozone Bodyglide Gel, Erozone Latex Dressing, Erozone Bodyglide Natural Foam, R & K International Cosmetics (2005) Summary page 1.
- K062796: K-Y Brand Intrigue, Personal Products Co. (2006) Summary page 1.
- K130012: Wet Platinum Personal Lubricant, Trigg Laboratories, Inc. (2013) Summary page 1.

## Indications for use
pjur™ Silicone Gel, pjur® Basic Personal Glide, pjur® Light, pjur® Med Premium Glide are personal lubricants, for genital area application. Intended to moisturize and lubricate, enhance the ease and comfort of intimate sexual activity and supplement the body's natural lubrication. These products are compatible with natural latex, polyurethane, and polylsoprene condoms.

Source page: https://510kreport.com/device/K133336
Methodology: https://510kreport.com/methodology