# Steris C/O Medical Device Consultants, Inc.

- Location (FDA's records): North Attleboro, MA
- FDA decisions: 1 (1988–1988): 1 510(k) clearance
- Product codes: MED (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- STERIS Corporation: 1 (https://510kreport.com/company/steris)
- Cottrell, Ltd.: 1 (https://510kreport.com/company/cottrell)
- Langford IC Systems, Inc.: 1 (https://510kreport.com/company/langford-ic-systems)
- Sterilox Technologies, Inc.: 1 (https://510kreport.com/company/sterilox-technologies)
- Advanced Sterilization Products: 1 (https://510kreport.com/company/advanced-sterilization-products)

## Its most-cited devices
- K875280: Steris System 1 Processor and 20 Sterilant (1988), cited by 5

## Recent decisions
- K875280: Steris System 1 Processor and 20 Sterilant (Sep 13, 1988)

Source page: https://510kreport.com/company/steris-c-o-medical-device-consultants