FDA applicant

Micron Precision Engineering, Inc.

San Pedro, CA2 decisions2000–20020 recalls

FDA records 2 decisions for Micron Precision Engineering, Inc. (San Pedro, CA) from 2000 to 2002: 2 510(k) clearances. Most are in product codes MNI (Orthosis, Spinal Pedicle Fixation) and KWP (Appliance, Fixation, Spinal Interlaminal). Its devices cite 1 predicate, 1 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, orthopedic panel, where it files most

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

FDA decisions per year

No FDA decision for Micron Precision Engineering, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micron Precision Engineering, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

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

Micron Precision Engineering, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Micron”