FDA applicant

Progressive Technology, Inc.

Mchenry, IL3 decisions1981–20150 recalls

FDA records 3 decisions for Progressive Technology, Inc. (Mchenry, IL) from 1981 to 2015: 3 510(k) clearances. Most are in product codes LDE (Stethoscope, Manual) and EJF (Bracket, Metal, Orthodontic). 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, dental panel, where it files most

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

FDA decisions per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Progressive Technology, 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 Concepts, Inc. 4 Progressive Productions, Ltd. 4 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 Technology, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Progressive”