FDA applicant

Micron Technology, Inc.

Boise, ID2 decisions1986–19920 recalls

FDA records 2 decisions for Micron Technology, Inc. (Boise, ID) from 1986 to 1992: 2 510(k) clearances. Most are in product codes NGE (Test, Luteinizing Hormone (Lh), Over The Counter) and GDX (Scalpel, One-Piece). 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, clinical chemistry panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micron 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 “Micron”

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

Micron Corp. 5 Micron Instruments, Inc. 3 Micron Precision Engineering, Inc. 2 Micron Metal & Plastic Manufactory Co. 2 Micron Surgical, Inc. 1 Micron Eyewear Manufactory Co., Ltd. 1 Micron Medical Corporation 1

Micron Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Micron”