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Data / Medical devices / China / Trolli King (holding) Ltd.

Trolli King (holding) Ltd.: FDA-registered device maker in Shenzhen Guangdong, China, 4 510(k) clearances

Trolli King (holding) Ltd. is registered with the FDA (registration 3003823002) in Shenzhen Guangdong, China. It lists 23 device types. The FDA files 4 510(k) clearances under its listings, the newest dated January 25, 2006. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3003823002
Address
No.5 Jiahu Road, Fuchengao Village PIN-HU TOWN, LONG-GANG DISTRICT, Shenzhen Guangdong, China, 518111
Owner or operator
TROLLI KING (HOLDING) LTD. (9090223)
Roles
Contract manufacturer, Exporter to the US, Manufacturer
First device listed
January 22, 2004
Registered through
2027
Brand names listed
AC-powered Adjustable Hospital Bed, ACCESSORIES, Adaptors, Anti tippers, Armrest, Bed, CVS HEALTH 3-IN-1 COMFORT COMMODE, CVS HEALTH CONVERTIBLE SHOWER CHAIR & STOOL and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Manufactureraccessdata.fda.gov
Adaptor, HygieneILS1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Aid, TransferIKX1Exporter to the US, Manufactureraccessdata.fda.gov
Armrest, WheelchairIML1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Manufactureraccessdata.fda.gov
Bed, ManualFNJ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Belt, WheelchairIQB1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Cane, Safety WalkKHY1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Chair, With CastersINM1Contract manufactureraccessdata.fda.gov
Climber, Curb, WheelchairIMN1Contract manufacturer, Exporter to the USaccessdata.fda.gov
Components, WheelchairKNN1Exporter to the US, Manufactureraccessdata.fda.gov
CrutchIPR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Cuff, Pusher, WheelchairINC1Exporter to the US, Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Footrest, WheelchairIMM1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Handrim, WheelchairIMO1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)HOY1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Stand, InfusionFOX1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Walker, MechanicalITJ1Contract manufacturer, Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Contract manufacturer, Exporter to the US, Manufactureraccessdata.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
January 25, 2006K053574MEDLINE PEDIATRIC WHEELCHAIRSIORSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
August 15, 2005K051302EXCEL BARIATRIC OR EXCEL SHUTTLE WHEELCHAIRIORSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
December 6, 2001K013761MEDLINE EXCEL RECLINCER WHEELCHAIRIORSubstantially EquivalentMedline Industries, Inc.accessdata.fda.gov
March 15, 1999K990463MEDLINE EXCEL WHEELCHAIRSIORSubstantially EquivalentMedlineaccessdata.fda.gov

Compare with other makers

Updated January 25, 2006. 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.