# Tri-Tech, Inc.

- Location (FDA's records): Fort Woth, TX
- FDA decisions: 11 (1981–1997): 11 510(k) clearances
- Product codes: ISD (4), JKA (3), FMH (1), DOF (1), BZD (1), JXA (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K971111: Tri-Tech Inc., Evacuated Blood Collection Tube, Gray Stopper (Jun 16, 1997)
- K952246: Tri-Techin. Custom Blood and/or Urine Transport Kit (Jun 20, 1995)
- K922343: Tri-Tech Inc. Custom Sexual Assault Kit (Feb 17, 1994)
- K922342: Tri-Tech Inc. Custom Blood Alcohol (Aug 27, 1993)
- K912140: Stairmaster Model 6000 Ergometer (Dec 17, 1991)
- K912057: 4000 PT Exercise System (Oct 24, 1991)
- K912056: Gravitron Upper Body System Exerciser (Oct 24, 1991)
- K912058: Gauntlet Stair Climber (Oct 24, 1991)

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