FDA applicant

Progressive Medical Technology, Inc.

Lansing, MI5 decisions1992–19930 recalls

FDA records 5 decisions for Progressive Medical Technology, Inc. (Lansing, MI) from 1992 to 1993: 5 510(k) clearances. Most are in product codes IRP (Massager, Powered Inflatable Tube) and IKZ (Bed, Patient Rotation, Powered). 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, physical medicine panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Progressive”

FDA records each applicant name separately; these may or may not be the same firm.

Progressive Electrical Therapeutics 10 Progressive Dynamics, Inc. 7 The Progressive Orthopaedic Company, LLC 5 Progressive Concepts, Inc. 4 Progressive Productions, Ltd. 4 Progressive Technology, Inc. 3 Progressive Surgical Products, Inc. 3 Progressive Wound Care Technologies, LLC 1 Progressive Affiliated Labs, Inc. 1 Progressive Medical, Inc. 1 Progressive Iv'S, Inc. 1 Progressive Optical Research, Ltd. 1

Progressive Medical Technology, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Progressive”