FDA applicant

Micron Instruments, Inc.

Walker, MI3 decisions1981–19840 recalls

FDA records 3 decisions for Micron Instruments, Inc. (Walker, MI) from 1981 to 1984: 3 510(k) clearances. 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 Micron Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micron Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micron Instruments, 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 “Micron”

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

Micron Corp. 5 Micron Precision Engineering, Inc. 2 Micron Technology, Inc. 2 Micron Metal & Plastic Manufactory Co. 2 Micron Surgical, Inc. 1 Micron Eyewear Manufactory Co., Ltd. 1 Micron Medical Corporation 1

Micron Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Micron”