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Data / Medical devices / Vietnam / Ever Global (vietnam) Enterprise Corporation

Ever Global (vietnam) Enterprise Corporation: FDA-registered device maker in Dong Nai Province, Vietnam, 2 510(k) clearances

Ever Global (vietnam) Enterprise Corporation is registered with the FDA (registration 3018108902) in Dong Nai Province, Vietnam. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 19, 2022. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3018108902
Address
Route 9, Giang Dien Industrial Zone An Vien Village, Dong Nai Province, Vietnam, 76320
Owner or operator
EVER GLOBAL (VIETNAM) ENTERPRISE CORPORATION (10090531)
Roles
Contract manufacturer, Manufacturer
First device listed
April 26, 2024
Registered through
2026
Brand names listed
Disposable Powder Free Vinyl Exam Glove, Clear/Yellow

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 19, 2022K220992Disposable Powder Free Vinyl Exam Glove, Black/Blue/PurpleLYZSubstantially EquivalentEver Global (Vietnam) Enterprise Corporationaccessdata.fda.gov
June 4, 2020K193555Disposable Powder Free Nitrile Examination Glove, Blue Color, Tested For Use With Chemotherapy Drugs and Fentanyl CitrateLZCSubstantially EquivalentEver Global (Vietnam) Enterprise Corpaccessdata.fda.gov

Compare with other makers

Updated October 19, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.