# J-Tech, Inc.

- Location (FDA's records): Midvale, UT
- FDA decisions: 5 (1991–1996): 5 510(k) clearances
- Product codes: KQX (2), LBB (1), HCC (1), FJL (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Stellate Systems: 1 (https://510kreport.com/company/stellate-systems)

## Its most-cited devices
- K945630: Large Muscle Strength Gauge (1995), cited by 1

## Recent decisions
- K954737: Surface Electromyograph Biofeedback Muscle Activity Device (Jul 3, 1996)
- K954647: Inclinometer (Oct 30, 1995)
- K945630: Large Muscle Strength Gauge (May 10, 1995)
- K913587: Jtech 50 Series Cutting Loop (Oct 23, 1991)
- K912526: GS-220 Hand Impairment Evaluation System (Sep 5, 1991)

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