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Data / Medical devices / United States / Usa Yanjan LLC

Usa Yanjan LLC: FDA-registered device maker in Statesville, NC, United States, 1 510(k) clearance

Usa Yanjan LLC is registered with the FDA (registration 3026612204) in Statesville, NC, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 27, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3026612204
Address
151 Walker Road, Statesville, NC, United States, 28625
Owner or operator
USA Yanjan LLC (10087494)
Roles
Repackager or relabeler
First device listed
March 6, 2023
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Tampon, Menstrual, Scented, Scented-DeodorizedHIL2Repackager or relabeleraccessdata.fda.gov
Tampon, Menstrual, UnscentedHEB2Repackager 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
June 27, 2008K081555TAMPAX PEARL PLASTIC APPLICATOR TAMPONS, SCENTED AND UNSCENTEDHILSubstantially EquivalentProcter & Gamble Co.accessdata.fda.gov

Compare with other makers

Updated June 27, 2008. 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.