FDA applicant

Progressive Concepts, Inc.

Denton, MD4 decisions1994–19950 recalls

FDA records 4 decisions for Progressive Concepts, Inc. (Denton, MD) from 1994 to 1995: 4 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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, neurology panel, where it files most

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

FDA decisions per year

No FDA decision for Progressive Concepts, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Medical Technology, Inc. 5 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 Concepts, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Progressive”