FDA applicant

Shamrock Manufacturing Company

Chino, CA2 decisions2001–20030 recalls

FDA records 2 decisions for Shamrock Manufacturing Company (Chino, CA) from 2001 to 2003: 2 510(k) clearances. All are in product code LZA (Polymer Patient Examination Glove). 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 hospital panel, where it files most

How often FDA has decided Shamrock Manufacturing Company’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Shamrock Manufacturing Company since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Shamrock Manufacturing Company’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

Other applicant names beginning “Shamrock”

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

Shamrock Marketing Co. 1

Shamrock Manufacturing Company

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Shamrock”