# Unomedical Sdn Bhd

- Location (FDA's records): West Malaysia, MY
- FDA decisions: 9 (1995–1998): 9 510(k) clearances
- Product codes: BTR (7), EZL (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Arcadia Medical Corporation: 2 (https://510kreport.com/company/arcadia-medical)
- Portex, Inc.: 1 (https://510kreport.com/company/portex)
- Flexicare Medical Limited.: 1 (https://510kreport.com/company/flexicare-medical)

## Its most-cited devices
- K954750: Pediatric Wire Reinforced Silicone Endotracheal Tube (1995), cited by 1
- K962389: Euromedical Reinforced Endotracheal Tube (1996), cited by 1
- K951696: Endotracheal Tube (1995), cited by 1
- K954754: Wire Reinforced Silicone Endotracheal Tube (1995), cited by 1

## Recent decisions
- K973076: Euromedical Haematuria Foley Catheter (Sep 16, 1998)
- K962389: Euromedical Reinforced Endotracheal Tube (Nov 21, 1996)
- K954750: Pediatric Wire Reinforced Silicone Endotracheal Tube (Dec 8, 1995)
- K954753: Pediatric Silicone Endotracheal Tube (Dec 8, 1995)
- K954751: Silicone Endotracheal Tube (Dec 8, 1995)
- K954754: Wire Reinforced Silicone Endotracheal Tube (Dec 8, 1995)
- K951696: Endotracheal Tube (May 22, 1995)
- K951697: Pediatric Endotracheal Tube (May 22, 1995)

Source page: https://510kreport.com/company/unomedical-sdn-bhd