FDA applicant

The Austin-Lenick Co.

Ft. Myers, FL1 decision1987–19870 recalls

FDA records 1 decision for The Austin-Lenick Co. (Ft. Myers, FL) in 1987: 1 510(k) clearance. All are in product code IPF (Stimulator, Muscle, 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 The Austin-Lenick Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Austin-Lenick Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — The Austin-Lenick Co. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “The”

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

Austin Biological Laboratories 45 Austin Miller Trauma, LLC 1 Austin Assoc. 1 Austin Medical, Inc. 1 Austin & Associates, Inc./Telos Medical Equipment 1 Austin Medical Ventures, Inc. 1

The Austin-Lenick Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”