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Data / Medical devices / Taiwan / Taiwan King Strong Co., Ltd.

Taiwan King Strong Co., Ltd.: FDA-registered device maker in Taichung City, Taiwan, 4 510(k) clearances

Taiwan King Strong Co., Ltd. is registered with the FDA (registration 3004141004) in Taichung City, Taiwan. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 4, 2004. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004141004
Address
No.144, Dong Ming Road Dajia District, Taichung City, Taiwan, 43773
Owner or operator
TAIWAN KING STRONG CO., LTD. (9058445)
Roles
Exporter to the US, Manufacturer
First device listed
November 29, 2006
Registered through
2026
Brand names listed
TAIWAN KING STRONG, Wheelchair Accessories

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the US, Manufactureraccessdata.fda.gov
Components, WheelchairKNN1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter to the US, Manufactureraccessdata.fda.gov
Wheelchair, PoweredITI2Exporter 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
November 4, 2004K042652TAIWAN KING STRONG TC 04 MECHANICALWHEELCHAIRIORSubstantially EquivalentTaiwan King Strong Co., Ltd.accessdata.fda.gov
December 2, 2003K033100TAIWAN KING STRONG POWERED WHEELCHAIR, TP 01ITISubstantially EquivalentTaiwan King Strong Co., Ltd.accessdata.fda.gov
December 2, 2003K033031TAIWAN KING STRONG TC 03 MECHANICAL WHEELCHAIRIORSubstantially EquivalentTaiwan King Strong Co., Ltd.accessdata.fda.gov
November 12, 2003K033097TAIWAN KING STRONG POWERED WHEELCHAIR, TP 02ITISubstantially EquivalentTaiwan King Strong Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 4, 2004. 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.