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Data / Medical devices / United States / Larada Sciences Inc.

Larada Sciences Inc.: FDA-registered device maker in Salt Lake City, UT, United States, 1 510(k) clearance

Larada Sciences Inc. is registered with the FDA (registration 3008501109) in Salt Lake City, UT, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 16, 2009. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3008501109
Address
4873 S State St, Salt Lake City, UT, United States, 84107
Owner or operator
Larada Sciences (10032545)
Roles
Specification developer
First device listed
May 24, 2010
Registered through
2026
Brand names listed
AirAlle, LRK, OneCure

Devices it lists

DeviceProduct codeClassRoleSource
Detectors And Removers, Lice, (Including Combs)LJL1Specification developeraccessdata.fda.gov
Lice Removal Kit Containing A SolutionPUN1Specification 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
December 16, 2009K093144LOUSEBUSTERLJLSubstantially EquivalentLarada Sciencesaccessdata.fda.gov

Compare with other makers

Updated December 16, 2009. 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.