FDA applicant

Micro Stamping Corp.

Maineville, OH1 decision2001–20010 recalls

FDA records 1 decision for Micro Stamping Corp. (Maineville, OH) in 2001: 1 510(k) clearance. All are in product code FZP (Clip, Implantable). 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, general and plastic surgery panel, where it files most

How often FDA has decided Micro Stamping Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Micro Stamping Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Micro Stamping Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Micro Stamping Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Micro Stamping Corp.

Which product codes does it file in?

What has FDA decided for it lately?