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Motion Control, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3001237006

Motion Control, Inc. is a medical device manufacturer, with 5 devices listed in FDA 510(k) and FDA GUDID (FDA Class II and I) and 1 FDA recall as of 13 Nov 2026.

Devices
5
Registrations
FDA
FDA recalls
1

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA 510(k) 4
  • FDA GUDID 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 3
  • FDA Class I 1
FDA recalls
Identifiers
  • FDA FEI 3001237006

Catalogue5

Newest first, rows 1-5 of 5

  • Myolab Ii Mc-200

    Listed Registry: GUDID Class:II

  • Dermatron Iontophoresis Device Ref K780310

    Active Regimes: 510(k) Registry: 510(k) Class:—

  • Phoresor Ii (Tm), Model PM700 Ref K872040

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Myolab Ii, Model Ml-200 Ref K862236

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Utah Artifical Arm Ref K802642

    Active Regimes: 510(k) Registry: 510(k) Class:I

Company details

FDA FEI number
3001237006
Address
115 N WRIGHT BROTHERS DR, SALT LAKE CITY, UT, 84116

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

  • 2005

    • 1 Feb 2005 Z-0959-05 Unclassified (pre-2012) Terminated Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard. Distribution: CA, DC, FL, NJ, OH, PA, SC, TN, TX, and Puerto Rico. No military, government or foreign distribution.

Frequently asked questions

How many devices does MOTION CONTROL, INC. have in the registry?

The registry currently lists 5 devices for MOTION CONTROL, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list MOTION CONTROL, INC.'s devices?

Among its 5 most recently registered devices, MOTION CONTROL, INC. has devices listed in FDA 510(k) (4 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do MOTION CONTROL, INC.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for MOTION CONTROL, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for MOTION CONTROL, INC.?

FDA recall records list 1 recall initiated by MOTION CONTROL, INC., the most recent initiated on 1 Feb 2005. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from MOTION CONTROL, INC. in the registry?

The most recently registered devices listed for MOTION CONTROL, INC. include MYOLAB II MC-200, DERMATRON IONTOPHORESIS DEVICE, PHORESOR II (TM), MODEL PM700 and MYOLAB II, MODEL ML-200.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company.