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Data / Medical devices / Taiwan / Aht Enterprise Corporation

Aht Enterprise Corporation: FDA-registered device maker in Hsinchu Hsinchu(County), Taiwan, 1 510(k) clearance

Aht Enterprise Corporation is registered with the FDA (registration 3023189540) in Hsinchu Hsinchu(County), Taiwan. It lists 21 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 13, 2012. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Aht Enterprise Corporation
FDA registration number
3023189540
Address
4F, No. 8, Lane 86, He Ping Road, Hsinchu Hsinchu(County), Taiwan, 300
Owner or operator
AHT Enterprise Corporation (10085047)
Roles
Exporter to the US, Manufacturer
First device listed
April 28, 2022
Registered through
2026
Brand names listed
ACCESSORIES, WHEELCHAIR, OXYGEN HOLDER, CANE & CRUTCH HOLDER (PLASTIC) tray table of wheelchair, ADAPTOR, HYGIENE, TOILET SEAT, TOILET SAFETY FRAME, AID, TRANSFER , BATH BENCH, SHOWER CHAIR, FOOT STOOL TUB RALL, GRAB BAR, ARMREST, WHEELCHAIR, ATTACHMENT, COMMODE, WHEELCHAIR, BRAKE, EXTENSION, WHEELCHAIR, CANE, CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT), E-RACK, OXYGEN CART, OXYGEN BAG, NEBULIZER BAG and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, WheelchairKNO1Exporter to the USaccessdata.fda.gov
Adaptor, HygieneILS1Exporter to the USaccessdata.fda.gov
Aid, TransferIKX1Exporter to the USaccessdata.fda.gov
Armrest, WheelchairIML1Exporter to the USaccessdata.fda.gov
Attachment, Commode, WheelchairINB1Exporter to the USaccessdata.fda.gov
Belt, WheelchairIQB1Exporter to the USaccessdata.fda.gov
Board, Lap, WheelchairIMX1Exporter to the USaccessdata.fda.gov
Brake, Extension, WheelchairIMW1Exporter to the USaccessdata.fda.gov
CaneIPS1Exporter to the USaccessdata.fda.gov
Cart, Emergency, Cardiopulmonary (Excluding Equipment)BZN1Exporter to the USaccessdata.fda.gov
Chair, Adjustable, MechanicalINN1Exporter to the USaccessdata.fda.gov
Components, WheelchairKNN1Exporter to the USaccessdata.fda.gov
CrutchIPR1Exporter to the USaccessdata.fda.gov
Device, Anti-Tip, WheelchairIMR1Exporter to the USaccessdata.fda.gov
Exerciser, Non-MeasuringION1Manufactureraccessdata.fda.gov
Footrest, WheelchairIMM1Exporter to the USaccessdata.fda.gov
Handrim, WheelchairIMO1Exporter to the USaccessdata.fda.gov
Stand, InfusionFOX1Exporter to the USaccessdata.fda.gov
Table, MechanicalINW1Exporter to the USaccessdata.fda.gov
Walker, MechanicalITJ1Exporter to the USaccessdata.fda.gov
Wheelchair, MechanicalIOR1Exporter 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
April 13, 2012K120032MECHANICAL WHEELCHAIRIORSubstantially EquivalentAikin Healthcare Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated April 13, 2012. 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.