# Tri W-G, Inc.

- Location (FDA's records): Valley City, ND
- FDA decisions: 35 (1979–1996): 35 510(k) clearances
- Product codes: INQ (14), IXR (3), IMC (2), BXB (2), ISD (2), JFB (2), IRQ (1), IOL (1), ITH (1), GZJ (1), INK (1), LGX (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
- K960196: Tri W-G, Inc Table, Tilt/Exam/Treatment Model 777 (Feb 7, 1996)
- K945163: Echocardiography (Feb 17, 1995)
- K941720: Model 747 and 747-30 Exam/Treatment Table (May 6, 1994)
- K936303: Treatment Table Modification (Mar 18, 1994)
- K933119: HI-LO Treatment Tables (Oct 12, 1993)
- K932746: Model T4501,T4502,T4503,T4504,T4504 Tilt Table (Jul 21, 1993)
- K930802: Models 642 & 643 Tilt Exam/Treatment Table (Mar 22, 1993)
- K925594: MDL 29001 Medi Elec-Mech Tilt Exam/Treatment Table (Feb 12, 1993)

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