# Vitaid, Ltd.

- Location (FDA's records): Ontario, Canada, CA
- FDA decisions: 7 (1989–2005): 7 510(k) clearances
- Product codes: BTR (3), EZL (1), CBI (1), KPM (1), KOD (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 4 (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 whose devices it cites most
- Mallinckrodt Critical Care: 1 (https://510kreport.com/company/mallinckrodt-critical-care)

## Firms that cite its devices most
- Kimberly-Clark Corp.: 2 (https://510kreport.com/company/kimberly-clark)
- Fuji Systems Corp.: 1 (https://510kreport.com/company/fuji-systems)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K050803: Pediatric Cuffed and Uncuffed ET Tubes; Standard Cuffed and Uncuffed ET Tubes (2005), cited by 2
- K894337: Univent Tube 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM (1989), cited by 1
- K932647: Wire Reinforced Endotracheal Tube (1993), cited by 1

## Recent decisions
- K050803: Pediatric Cuffed and Uncuffed ET Tubes; Standard Cuffed and Uncuffed ET Tubes (Jun 30, 2005)
- K932647: Wire Reinforced Endotracheal Tube (Nov 2, 1993)
- K901738: Selfcath (Jun 27, 1990)
- K894883: Phycon All Silicone Balloon Catheter (Apr 25, 1990)
- K894794: Agishi Ascites Pump Peritoneocaval Shunt Pump (Nov 21, 1989)
- K894669: Laser Shielding Tube (Oct 13, 1989)
- K894337: Univent Tube 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM (Sep 29, 1989)

Source page: https://510kreport.com/company/vitaid