RegWardenFDA facility compliance records
Facility

EMG TECHNOLOGY CO., LTD.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2014: 1 recalls; 2017: 1 inspections; 2024: 1 inspections1’14’15’161’17’18’19’20’21’22’231’24’25’26
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

  • Apparatus, Suction, Ward Use, Portable, Ac-Powered
    Product code JCX (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4780

Recalls & enforcement

FDA inspections (2)

  • VAI2024-12-13
    Voluntary Action Indicated · Compliance: Devices
  • NAI2017-08-17
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “EMG TECHNOLOGY CO., LTD. (FEI 3003803075) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003803075-emg-technology-co-ltd/

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