510(k) Report

FDA applicant

Dong Bang, U.S.A.

Santa Fe Springs, CA2 decisions1997–19970 recalls

FDA records 2 decisions for Dong Bang, U.S.A. (Santa Fe Springs, CA) in 1997: 2 510(k) clearances. 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 Dong Bang, U.S.A.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dong Bang, U.S.A. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dong Bang, U.S.A. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MQXNeedle, Acupuncture, Single Use2decisions

Who builds on its devices?

Later devices cite its devices 2 times; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K972659Dong Bang Acupuncture NeedlesDong Bang, U.S.A. · 19972cite it

What has FDA decided for it lately?

  • K972658Magi Acupuncture NeedlesDong Bang, U.S.A. · 1997
  • K972659Dong Bang Acupuncture NeedlesDong Bang, U.S.A. · 1997

All 2 as Dong Bang, U.S.A. →

Other applicant names beginning “Dong”

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

Dong IL Technology, Ltd. 2Dong-A Pharmaceutical Co., Ltd. 2Dong Guan OU Kang Electronics Co., Ltd. 1Dong Tai City Huayi Gloves Co., Ltd. 1Dong Guan Kinyet Metal Products Co., Ltd. 1Dong Nai Garment Corporation (Donagamex) 1