FDA applicant

Promatek Medical Systems, Inc.

Joliet, IL1 decision1990–19900 recalls

FDA records 1 decision for Promatek Medical Systems, Inc. (Joliet, IL) in 1990: 1 510(k) clearance. All are in product code IKK (System, Isokinetic Testing And Evaluation). 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 Promatek Medical Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Promatek Medical Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Promatek Medical Systems, 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 “Promatek”

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

Promatek Industries, Ltd. 3 Promatek 1

Promatek Medical Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Promatek”