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Data / Medical devices / United States / Mediprime Supply Inc.

Mediprime Supply Inc.: FDA-registered device maker in Madera, CA, United States, 1 510(k) clearance

Mediprime Supply Inc. is registered with the FDA (registration 3045323828) in Madera, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 16, 2002. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3045323828
Address
335 S Schnoor Ave Ste 117, Madera, CA, United States, 93637
Owner or operator
Mediprime Supply Inc. (10095612)
Roles
Complaint file establishment, Repackager or relabeler
First device listed
April 2, 2026
Registered through
2026
Brand names listed
MediPrime Supply

Devices it lists

DeviceProduct codeClassRoleSource
Vinyl Patient Examination GloveLYZ1Complaint file establishment, 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
September 16, 2002K022600POWDER FREE SYNTHETIC VINYL EXAMINATION GLOVESLYZSubstantially EquivalentShijiazhuang Wally Plastics Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated September 16, 2002. 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.