# Medical Instruments Technology, Inc.

- Location (FDA's records): St. George, UT
- FDA decisions: 5 (1989–2002): 5 510(k) clearances
- Product codes: HRX (2), KCY (1), KQX (1), JOW (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Instrumed, Inc.: 1 (https://510kreport.com/company/instrumed)
- Dyonics, Inc.: 1 (https://510kreport.com/company/dyonics)
- Mitek Products: 1 (https://510kreport.com/company/mitek-products)
- Arthrocare Corp.: 1 (https://510kreport.com/company/arthrocare)

## Firms that cite its devices most
- Compression Works, LLC: 1 (https://510kreport.com/company/compression-works)

## Its most-cited devices
- K012632: Tourniquet Cuff; Pneumatic Tourniquet (2001), cited by 1

## Recent decisions
- K012614: Kendall, Sequential Compression Device; Huntleigh, Flowtron; Venaflow; Acufex; Alps; Sheepskin (May 1, 2002)
- K012640: Electrosurgical Cutting and Coagulation Accessories, Electrosurgical Wands (Feb 28, 2002)
- K012624: Reprocessed Arthroscopic Blades, Arthroscopic Shavers, Shaver Blade, Blade, Limited Reuse Blade, Arthroscopic Burs (Nov 8, 2001)
- K012632: Tourniquet Cuff; Pneumatic Tourniquet (Oct 26, 2001)
- K884611: The Orthoranger II Electronic Goniometer (Jan 31, 1989)

Source page: https://510kreport.com/company/medical-instruments-technology