510(k) Report

FDA applicant

K.S. Choi Corporation

Los Angeles, CA2 decisions1996–20150 recalls

FDA records 2 decisions for K.S. Choi Corporation (Los Angeles, CA) from 1996 to 2015: 2 510(k) clearances. All are in product code MQX (Needle, Acupuncture, Single Use). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “K.S. Choi Corp.”.

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 K.S. Choi Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2015: 1
2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — K.S. Choi Corporation by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like K.S. Choi Corporation’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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Which product codes does it file in?

  • MQXNeedle, Acupuncture, Single Use2decisions

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K142760Acuzone Acupuncture Needles, KSC DB Plus Acupuncture NeedlesK.S. Choi Corporation · 2015
  • K961677Acupuncture NeedlesK.S. Choi Corp. · 1996

The one decision as K.S. Choi Corporation →The one decision as K.S. Choi Corp. →