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Data / Medical devices / United States / KM Supplies

KM Supplies: FDA-registered device maker in Los Angeles, CA, United States, 2 510(k) clearances

KM Supplies is registered with the FDA (registration 3008400688) in Los Angeles, CA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 11, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3008400688
Address
1132 Crenshaw Blvd, Los Angeles, CA, United States, 90019
Owner or operator
KM Supplies (10040673)
Roles
Specification developer
First device listed
February 22, 2024
Registered through
2026
Brand names listed
KM Acupuncture Needle, Single Use, KMA Acupuncture Needle, Single Use

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Acupuncture, Single UseMQX2Specification developeraccessdata.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
May 11, 2017K162566AIK Sterile Acupuncture Needles for Single UseMQXSubstantially EquivalentChangchun Aik Medical Devices Co., Ltd.accessdata.fda.gov
June 10, 2015K142920KM Needles (Acupuncture Needle)MQXSubstantially EquivalentK.M.S., Inc.accessdata.fda.gov

Compare with other makers

Updated May 11, 2017. 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.