# Pharma-Plast USA, Inc.

- Location (FDA's records): Canada  H3a 2n4, CA
- FDA decisions: 9 (1985–1989): 9 510(k) clearances
- Product codes: FMI (3), FMF (2), DZM (1), LZG (1), BTR (1), FOZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- Mentor Medical Limited: 1 (https://510kreport.com/company/mentor-medical)

## Its most-cited devices
- K852444: Asik 'Once' Syringe (1985), cited by 1

## Recent decisions
- K894371: Nipro Safelet Cath (Oct 25, 1989)
- K894373: Nipro Dental Needle (Oct 13, 1989)
- K894374: Blood Drawing Needle (Sep 28, 1989)
- K894372: Nipro Needle Holder (Sep 28, 1989)
- K884978: Pharma-Plast Insulin Infusion Set (Jun 21, 1989)
- K871263: Multiple Pharma-Plast Tracheal Tube (Jun 15, 1987)
- K852443: Pharma-Plast Clinipak (Oct 16, 1985)
- K852444: Asik 'Once' Syringe (Oct 16, 1985)

Source page: https://510kreport.com/company/pharma-plast-usa
