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Data / Medical devices / United States / Convaid Products LLC

Convaid Products LLC: FDA-registered device maker in Torrance, CA, United States, 5 510(k) clearances

Convaid Products LLC is registered with the FDA (registration 2022883) in Torrance, CA, United States. It lists 4 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 18, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2022883
Address
2830 California St, Torrance, CA, United States, 90503
Owner or operator
Convaid Products, LLC (10056491)
Roles
Manufacturer, Repackager or relabeler, Specification developer
First device listed
December 14, 2017
Registered through
2026
Brand names listed
Coaster 12, Coaster 12 Scout, Coaster 12 Transit, Coaster 14, Coaster 14 Scout, Coaster 14 Scout Transit, Coaster 14 Transit, Coaster 16 and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Manufacturer, Repackager or relabeler, Specification developeraccessdata.fda.gov
Chair, With CastersINM1Manufactureraccessdata.fda.gov
Stroller, AdaptiveLBE1Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Manufactureraccessdata.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
October 18, 2017K171017Convaid Flyer FL12, FL13, FL14, FL15 and FL16; Convaid Flyer transit FL12T, FL13T, FL14T, FL15T and FL16TIORSubstantially EquivalentConvaid Products, LLCaccessdata.fda.gov
September 17, 2014K140416TREKKER, TREKKER TRANSITIORSubstantially EquivalentConvaid Products, Inc.accessdata.fda.gov
September 24, 2003K032402RODEO MODEL, RD12, RD14, RD16, RADIO TRANSIT MODEL, RD12T, RD14T, RD16T,IORSubstantially EquivalentConvaid Products, Inc.accessdata.fda.gov
October 27, 1982K822992PEOPLE MOVERINMSubstantially EquivalentConvaid Products, Inc.accessdata.fda.gov
March 26, 1981K810676CONVAID CRUISER CP4MLBESubstantially EquivalentConvaid Products, Inc.accessdata.fda.gov

Compare with other makers

Updated October 18, 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.