510(k) Report

FDA applicant

United Pacific Co., Ltd.

Alhambra, CA6 decisions1999–20030 recalls

FDA records 6 decisions for United Pacific Co., Ltd. (Alhambra, CA) from 1999 to 2003: 6 510(k) clearances. Most are in product codes MQX (Needle, Acupuncture, Single Use) and ILY (Lamp, Infrared, Therapeutic Heating). No recall is linked to its devices.

FDA’s records also spell it “United Pacific, Inc.”.

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 United Pacific Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for United Pacific Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — United Pacific Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like United Pacific Co., Ltd.’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