# Tri-Ject Intl. Corp.

- Location (FDA's records): Puyallup, WA
- FDA decisions: 1 (2000–2000): 1 510(k) clearance
- Product codes: MEG (1)
- 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
- M.K. Meditech Co., Ltd.: 2 (https://510kreport.com/company/mk-meditech)
- U.S. Technologies, Inc.: 1 (https://510kreport.com/company/us-technologies)
- Terumo Europe N.V.: 1 (https://510kreport.com/company/terumo-europe)

## Its most-cited devices
- K000572: E.N.S.I. Syringe (2000), cited by 4

## Recent decisions
- K000572: E.N.S.I. Syringe (Feb 24, 2000)

Source page: https://510kreport.com/company/tri-ject-intl