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Data / Medical devices / United States / Raja Trading Company, Inc.

Raja Trading Company, Inc.: FDA-registered device maker in Fairfax, VA, United States, 3 510(k) clearances

Raja Trading Company, Inc. is registered with the FDA (registration 3017060146) in Fairfax, VA, United States. It lists 5 device types. The FDA files 3 510(k) clearances under its listings, the newest dated February 10, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3017060146
Address
2801 Juniper Street Suite 2, Fairfax, VA, United States, 22031
Owner or operator
RAJA Trading Company, Inc. (10075612)
Roles
Manufacturer, Repackager or relabeler
First device listed
June 20, 2020
Registered through
2026
Brand names listed
Ionixlight, Juvesa Proskin, MyoLight Microcurrent Handle, OxyLight, OxyLight Ionix, Oxylight

Devices it lists

DeviceProduct codeClassRoleSource
Brush, Dermabrasion, PoweredGFE1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Massager, Therapeutic, ElectricISA1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Powered Laser Surgical InstrumentGEX2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Stimulator, Muscle, PoweredIPF2Manufacturer, Repackager or relabeleraccessdata.fda.gov
Stimulator, Transcutaneous Electrical, Aesthetic PurposesNFO2Manufacturer, Repackager or relabeleraccessdata.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
February 10, 2025K243063Myolight Microcurrent HandpieceNFOSubstantially EquivalentRaja Trading Company, Inc.accessdata.fda.gov
December 2, 2021K202175OxyLight 2.0GEXSubstantially EquivalentRaja Trading Company, Inc.accessdata.fda.gov
June 4, 2020K200104OxylightGEXSubstantially EquivalentRaja Trading Company, Inc.accessdata.fda.gov

Compare with other makers

Updated February 10, 2025. 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.