# Reckitt Benckiser, LLC

- Location (FDA's records): Parsippany, NJ
- FDA decisions: 9 (1996–2018): 9 510(k) clearances
- Names in FDA's records: Reckitt Benckiser, LLC (5); Reckitt Benckiser, Inc. (3); Reckitt Benckiser (1)
- Product codes: NUC (6), MED (2), LRJ (1)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 7 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mcneil-Ppc, Inc.: 2 (https://510kreport.com/company/mcneil-ppc)
- One: 2 (https://510kreport.com/company/one)
- Johnson & Johnson Medical, Inc.: 1 (https://510kreport.com/company/johnson-johnson-medical)
- Ortho Pharmaceutical Corp.: 1 (https://510kreport.com/company/ortho-pharmaceutical)

## Firms that cite its devices most
- Nanosonics Limited: 1 (https://510kreport.com/company/nanosonics)
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Neo Cosmetique: 1 (https://510kreport.com/company/neo-cosmetique)
- Rb Health (Us), LLC: 1 (https://510kreport.com/company/rb-health-us)
- Thai Nippon Rubber Industry Public Company Limited.: 1 (https://510kreport.com/company/thai-nippon-rubber-industry-public)

## Its most-cited devices
- K970230: Sporox (1997), cited by 3
- K151884: K-Y Marilyn Pleasure Gel (2016), cited by 2
- K140193: Durex Embrace Personal Lubricant (2014), cited by 1
- K173504: K-Y Silicone (2018), cited by 1

## Recent decisions
- K173504: K-Y Silicone (Jan 12, 2018)
- K151884: K-Y Marilyn Pleasure Gel (Jan 11, 2016)
- K143532: Durex Silicone (Jul 31, 2015)
- K143511: K-Y BRAND TOUCH All-in-one Warming Caressing Creme and Personal Lubricant (May 20, 2015)
- K131643: Durex Realfeel Pleasure Gel Personal Lubricant (Dec 17, 2014)
- K140193: Durex Embrace Personal Lubricant (Nov 4, 2014)
- K990703: Sporox II Sterilizing & Disinfecting Solution (Mar 30, 1999)
- K970230: Sporox (Oct 29, 1997)

Source page: https://510kreport.com/company/reckitt-benckiser