510(k) Report

FDA applicant

Medical Technology and Innovations, Inc.

Lee'S Summit, MO3 decisions1986–20020 recalls

FDA records 3 decisions for Medical Technology and Innovations, Inc. (Lee'S Summit, MO) from 1986 to 2002: 3 510(k) clearances. Most are in product codes HHW (Pessary, Vaginal) and MMF (Photorefractor). Its devices cite 1 predicate, 0 of them its own earlier devices. No 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Medical Technology and Innovations, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • HHWPessary, Vaginal1decision
  • MMFPhotorefractor1decision
  • BXBExerciser, Powered1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K020512Mti ST#1 Silicone PessaryMedical Technology and Innovations, Inc. · 2002
  • K934880Mti PhotoscreenerMedical Technology and Innovations, Inc. · 1994
  • K854354The Bledsoe Passive Motion ExerciserMedical Technology and Innovations, Inc. · 1986

All 3 as Medical Technology and Innovations, Inc. →