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Data / Medical devices / Taiwan / CC Hsing Company Limited

CC Hsing Company Limited: FDA-registered device maker in Xikou Township Chiayi(County), Taiwan, 4 510(k) clearances

CC Hsing Company Limited is registered with the FDA (registration 3014273557) in Xikou Township Chiayi(County), Taiwan. It lists 32 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 26, 2007. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch CC Hsing Company Limited
FDA registration number
3014273557
Address
NO.1,BENTING Xikou Township, Xikou Township Chiayi(County), Taiwan, 62348
Owner or operator
TAIWAN AN I CO.,LTD. (9021165)
Roles
Exporter to the US
First device listed
March 27, 2002
Registered through
2026
Brand names listed
AMG Medical, AMG USA, ARM PAD.DSK-PMT XD (90762911), Airgo, Alevo, Barton Medical Corporation, Breezy, Disposable Splint and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, HygieneILS1Exporter to the USaccessdata.fda.gov
Aid, TransferIKX1Exporter to the USaccessdata.fda.gov
Apparatus, Traction, Non-PoweredHST1Exporter to the USaccessdata.fda.gov
Armrest, WheelchairIML1Exporter to the USaccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Exporter to the USaccessdata.fda.gov
Bed, ManualFNJ1Exporter to the USaccessdata.fda.gov
Belt, WheelchairIQB1Exporter to the USaccessdata.fda.gov
CaneIPS1Exporter to the USaccessdata.fda.gov
Cane, Safety WalkKHY1Exporter to the USaccessdata.fda.gov
Chair And Table, MedicalKMN1Exporter to the USaccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Exporter to the USaccessdata.fda.gov
Chair, Blood DonorFML1Exporter to the USaccessdata.fda.gov
Chair, Surgical, Non-ElectricalFZK1Exporter to the USaccessdata.fda.gov
Chair, With CastersINM1Exporter to the USaccessdata.fda.gov
CrutchIPR1Exporter to the USaccessdata.fda.gov
Cushion, WheelchairIMP1Exporter to the USaccessdata.fda.gov
Exerciser, Non-MeasuringION1Exporter to the USaccessdata.fda.gov
Footrest, WheelchairIMM1Exporter to the USaccessdata.fda.gov
Halter, Head, TractionHSS1Exporter to the USaccessdata.fda.gov
Handrim, WheelchairIMO1Exporter to the USaccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Exporter to the USaccessdata.fda.gov
Lift, Patient, Non-Ac-PoweredFSA1Exporter to the USaccessdata.fda.gov
Operating Room Accessories Table TrayFWZ1Exporter to the USaccessdata.fda.gov
Pump, Portable, Aspiration (Manual Or Powered)BTA2Exporter to the USaccessdata.fda.gov
Regulator, Pressure, Gas CylinderCAN1Exporter to the USaccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Exporter to the USaccessdata.fda.gov
Stand, InfusionFOX1Exporter to the USaccessdata.fda.gov
Tips And Pads, Cane, Crutch And WalkerINP1Exporter to the USaccessdata.fda.gov
Tubing, Pressure And AccessoriesBYX1Exporter to the USaccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the USaccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter to the USaccessdata.fda.gov
Wheelchair, PoweredITI2Exporter to the USaccessdata.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 26, 2007K071607ASA01 HEAVY DUTY SUCTION PUMPBTASubstantially EquivalentZhongshan A&J Medical Equipment Co., Ltd.accessdata.fda.gov
December 9, 2005K052586A & I PEDIATRIC WHEELCHAIRS, MODELS RWAL2006-12, LT3207-12. A & I BARIATRIC WHEELCHAIRS, MODEL NO. WCDE2611P, WCDE2811PIORSubstantially EquivalentTaiwan an I Co., Ltd.accessdata.fda.gov
May 25, 2004K041190A&I POWER WHEELCHAIR, PC-401ITISubstantially EquivalentWell Success Biotech, Inc.accessdata.fda.gov
February 15, 2001K010094A & I WHEELCHAIRSIORSubstantially EquivalentTaiwan an I Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated June 26, 2007. 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.