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Data / Medical devices / United States / QPSI Mooresville

QPSI Mooresville: FDA-registered device maker in Mooresville, IN, United States, 1 510(k) clearance

QPSI Mooresville is registered with the FDA (registration 3009446098) in Mooresville, IN, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated February 20, 2002. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009446098
Address
9440 South State Route 39 Suite 1, Mooresville, IN, United States, 46158
Owner or operator
Quality Packaging Specialists International (9067895)
Roles
Repackager or relabeler
First device listed
April 25, 2017
Registered through
2026
Brand names listed
Band Aid tapes, bandages & adhesive

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, Soft Lens ProductsLPN2Repackager or relabeleraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Repackager 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 20, 2002K014202COMPLETE BRAND MULTI-PURPOSE SOLUTIONLPNSubstantially EquivalentAllergan, Inc.accessdata.fda.gov

Compare with other makers

Updated February 20, 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.