510(k) Report

FDA applicant

Medical Instruments Technology, Inc.

St. George, UT5 decisions1989–20021 recall

FDA records 5 decisions for Medical Instruments Technology, Inc. (St. George, UT) from 1989 to 2002: 5 510(k) clearances. Most are in product codes HRX (Arthroscope) and KCY (Tourniquet, Pneumatic). Its devices cite 4 predicates, 0 of them its own earlier devices. 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, orthopedic panel, where it files most

How often FDA has decided Medical Instruments Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Instruments Technology, Inc. since 2007.

Recalls per year

1in 2008

2008: 1
2007high 1 (2008) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Medical Instruments Technology, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medical Instruments Technology, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • HRXArthroscope2decisions
  • KCYTourniquet, Pneumatic1decision
  • KQXGoniometer, Ac-Powered1decision
  • JOWSleeve, Limb, Compressible1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K012632Tourniquet Cuff; Pneumatic TourniquetMedical Instruments Technology, Inc. · 20011cites it

What has FDA decided for it lately?

  • K012614Kendall, Sequential Compression Device; Huntleigh, Flowtron; Venaflow; Acufex; Alps; SheepskinMedical Instruments Technology, Inc. · 2002
  • K012640Electrosurgical Cutting and Coagulation Accessories, Electrosurgical WandsMedical Instruments Technology, Inc. · 20021 recall
  • K012624Reprocessed Arthroscopic Blades, Arthroscopic Shavers, Shaver Blade, Blade, Limited Reuse Blade…Medical Instruments Technology, Inc. · 2001
  • K012632Tourniquet Cuff; Pneumatic TourniquetMedical Instruments Technology, Inc. · 2001
  • K884611The Orthoranger II Electronic GoniometerMedical Instruments Technology, Inc. · 1989

All 5 as Medical Instruments Technology, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K012640Turbovac Suction Wand - Reprocessed Sterile device -- Orthopedic Arthroscope.Mar 11, 2008