# Motion Control, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (1978–1987): 4 510(k) clearances
- Product codes: EGJ (1), IKN (1), IRE (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 3 (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
- Empi: 2 (https://510kreport.com/company/empi)
- Eemso, Inc.: 1 (https://510kreport.com/company/eemso)

## Its most-cited devices
- K872040: Phoresor II (TM), Model PM700 (1987), cited by 2
- K780310: Dermatron Iontophoresis Device (1978), cited by 1

## Recent decisions
- K872040: Phoresor II (TM), Model PM700 (Aug 4, 1987)
- K862236: Myolab II, Model ML-200 (Aug 7, 1986)
- K802642: Utah Artifical Arm (Nov 12, 1980)
- K780310: Dermatron Iontophoresis Device (Jul 31, 1978)

Source page: https://510kreport.com/company/motion-control