510(k) Report

FDA applicant

Hummingbird Medical Technology, LLC

Allen, TX1 decision2001–20010 recalls

FDA records 1 decision for Hummingbird Medical Technology, LLC (Allen, TX) in 2001: 1 510(k) clearance. All are in product code MQX (Needle, Acupuncture, Single Use). 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 Hummingbird Medical Technology, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hummingbird Medical Technology, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hummingbird Medical Technology, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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