# Arcadia Medical Corporation

- Location (FDA's records): Appollo Beach, FL
- FDA decisions: 2 (2003–2006): 2 510(k) clearances
- Product codes: BTO (1), BTR (1)
- Predicates its devices cite: 8 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bivona Medical Technologies: 4 (https://510kreport.com/company/bivona-medical-technologies)
- Unomedical Sdn Bhd: 2 (https://510kreport.com/company/unomedical-sdn-bhd)
- Portex, Inc.: 1 (https://510kreport.com/company/portex)
- The Laryngeal Mask Co., Ltd.: 1 (https://510kreport.com/company/laryngeal-mask)

## Firms that cite its devices most
- Vitaltec Corporation: 1 (https://510kreport.com/company/vitaltec)

## Its most-cited devices
- K031553: Silicone Foam Cuff Tracheostomy Tubes, Silicone Cuffless Neonatal and Pediatric Tracheostomy Tubes (2003), cited by 1

## Recent decisions
- K060094: Arcadia Medical Silicone Wire Reinforced Endotracheal Tubes (May 8, 2006)
- K031553: Silicone Foam Cuff Tracheostomy Tubes, Silicone Cuffless Neonatal and Pediatric Tracheostomy Tubes (Nov 18, 2003)

Source page: https://510kreport.com/company/arcadia-medical