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Data / Medical devices / Cambodia / Ming Fai Enterprise (cambodia) Co.,ltd

Ming Fai Enterprise (cambodia) Co.,ltd: FDA-registered device maker in Samraong Tong District Kampong Speu, Cambodia, 1 510(k) clearance

Ming Fai Enterprise (cambodia) Co.,ltd is registered with the FDA (registration 3015531959) in Samraong Tong District Kampong Speu, Cambodia. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 9, 1985. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Ming Fai Enterprise (cambodia) Co.,ltd
FDA registration number
3015531959
Address
National Road 41(Preah Ang Duong Road), Veal Vong Village, Sen Dei Commune, Samraong Tong District Kampong Speu, Cambodia, 050109
Owner or operator
Ming Fai Enterprise (Cambodia) Co.,LTD (10060734)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
June 18, 2019
Registered through
2027
Brand names listed
CONTAINER, I.V, Drape, surgical, Hearing(insert), MICROSCOPE, OPERATING & ACCESSORIES, AC-POWERED, OPHTHALMIC, O.R. Table Sheets, Operating Room Accessories Table Tray, Probe covers, Protector and more

Devices it lists

DeviceProduct codeClassRoleSource
Applicator, Absorbent Tipped, Non-SterileKXF1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Container, I.V.KPE2Contract manufactureraccessdata.fda.gov
Dental Hygiene KitNXZ1Manufactureraccessdata.fda.gov
Drape, Surgical, AntimicrobialKKX2Contract manufactureraccessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella EuaQKRNManufactureraccessdata.fda.gov
Fiber, Medical, AbsorbentFRL1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Floss, DentalJES1Contract manufacturer, Manufacturer, Repackager or relabeleraccessdata.fda.gov
Microscope, Operating & Accessories, Ac-Powered, OphthalmicHRM1Contract manufactureraccessdata.fda.gov
Operating Room Accessories Table TrayFWZ1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Protector, Hearing (Insert)EWDURepackager or relabeleraccessdata.fda.gov
Protector, Skin PressureFMP1Repackager or relabeleraccessdata.fda.gov
Set, I.V. Fluid TransferLHI2Contract manufactureraccessdata.fda.gov
Stretcher, Patient RestraintNZD1Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
System, X-Ray, Fluoroscopic, Image-IntensifiedJAA2Contract manufacturer, Repackager or relabeleraccessdata.fda.gov
Toothbrush, ManualEFW1Manufactureraccessdata.fda.gov
Transducer, Ultrasonic, DiagnosticITX2Contract manufactureraccessdata.fda.gov

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
April 9, 1985K850959EQUIPMENT SNAP KOVERSJAASubstantially EquivalentAdvance Medical Designs, Inc.accessdata.fda.gov

Compare with other makers

Updated April 9, 1985. 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.