# Johnson & Johnson Consumer, Inc.

- Location (FDA's records): Fort Washington, PA
- FDA decisions: 2 (2018–2018): 2 510(k) clearances
- Product codes: OHS (1), OLP (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 7 (0 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
- Lg Electronics.Inc: 1 (https://510kreport.com/company/lg-electronics)
- Trophy Skin, Inc.: 1 (https://510kreport.com/company/trophy-skin)
- La Lumiere, LLC: 1 (https://510kreport.com/company/la-lumiere)
- Pulsaderm, LLC: 1 (https://510kreport.com/company/pulsaderm)

## Firms that cite its devices most
- Duplex International Trading Limited: 2 (https://510kreport.com/company/duplex-international-trading)
- Galactic Beauty, LLC: 2 (https://510kreport.com/company/galactic-beauty)
- Cellreturn Co., Ltd.: 1 (https://510kreport.com/company/cellreturn)
- Shenzhen Kaiyan Medical CO, Ltd.: 1 (https://510kreport.com/company/shenzhen-kaiyan-medical)
- Bemer Int AG: 1 (https://510kreport.com/company/bemer-int)

## Its most-cited devices
- K180847: Neutrogena Light Therapy Acne Mask+ (2018), cited by 4
- K180856: Neutrogena Light Therapy Aging Mask+ (2018), cited by 3

## Recent decisions
- K180856: Neutrogena Light Therapy Aging Mask+ (Jun 19, 2018)
- K180847: Neutrogena Light Therapy Acne Mask+ (Jun 19, 2018)

Source page: https://510kreport.com/company/johnson-johnson-consumer