# Sterilox Technologies, Inc.

- Location (FDA's records): Radnor, PA
- FDA decisions: 2 (2002–2006): 2 510(k) clearances
- Product codes: FRO (1), MED (1)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 2 (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
- Johnson & Johnson Medical, Inc.: 3 (https://510kreport.com/company/johnson-johnson-medical)
- Oculus Innovative Sciences: 2 (https://510kreport.com/company/oculus-innovative-sciences)
- Dpt Laboratories, Ltd.: 1 (https://510kreport.com/company/dpt-laboratories)
- Carrington Laboratories, Inc.: 1 (https://510kreport.com/company/carrington-laboratories)
- Dentsply Intl.: 1 (https://510kreport.com/company/dentsply-intl)
- Cottrell, Ltd.: 1 (https://510kreport.com/company/cottrell)
- Steris C/O Medical Device Consultants, Inc.: 1 (https://510kreport.com/company/steris-c-o-medical-device-consultants)

## Firms that cite its devices most
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Puricore, Inc.: 1 (https://510kreport.com/company/puricore)

## Its most-cited devices
- K013280: Sterilox Liquid Chemical Sterilant System (2002), cited by 2

## Recent decisions
- K060901: Vashe Wound Cleansing System (Jun 29, 2006)
- K013280: Sterilox Liquid Chemical Sterilant System (Sep 18, 2002)

Source page: https://510kreport.com/company/sterilox-technologies