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Data / Medical devices / Taiwan / Huntex Corporation

Huntex Corporation: FDA-registered device maker in Taipei, Taiwan, 2 510(k) clearances

Huntex Corporation is registered with the FDA (registration 1000328618) in Taipei, Taiwan. It lists 20 device types. The FDA files 2 510(k) clearances under its listings, the newest dated July 10, 2008. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Huntex Corporation
FDA registration number
1000328618
Address
No. 35-3 Lane 165 Hsin Sheng S. RD., Sec. 1, Taipei, Taiwan, 106
Owner or operator
HUNTEX CORPORATION (9011461)
Roles
Contract manufacturer, Manufacturer
First device listed
September 21, 1994
Registered through
2026
Brand names listed
Abdominal Binder, Ankle Brace or Support, Arm Sling, Cervical Orthosis, Clavicle Splint, Hand Splint, Hernia Support, Hot / Cold Water Bottle and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, TractionILZ1Manufactureraccessdata.fda.gov
Apparatus, Traction, Non-PoweredHST1Manufactureraccessdata.fda.gov
Band Or Belt, Pelvic SupportISR1Contract manufacturer, Manufactureraccessdata.fda.gov
Belt, Pelvic, TractionHSQ1Contract manufacturer, Manufactureraccessdata.fda.gov
Binder, AbdominalFSD1Contract manufacturer, Manufactureraccessdata.fda.gov
Bottle, Hot/Cold WaterFPF1Manufactureraccessdata.fda.gov
Cage, KneeITM1Manufactureraccessdata.fda.gov
Douche Apparatus, Vaginal, TherapeuticHED1Manufactureraccessdata.fda.gov
Halter, Head, TractionHSS1Manufactureraccessdata.fda.gov
Joint, Ankle, External BraceITW1Contract manufacturer, Manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Contract manufacturer, Manufactureraccessdata.fda.gov
Joint, Knee, External Limb ComponentISY1Manufactureraccessdata.fda.gov
Orthosis, CervicalIQK1Contract manufacturer, Manufactureraccessdata.fda.gov
Orthosis, Limb BraceIQI1Contract manufacturer, Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Manufactureraccessdata.fda.gov
Sling, ArmILI1Contract manufacturer, Manufactureraccessdata.fda.gov
Splint, ClavicleIQJ1Contract manufacturer, Manufactureraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Contract manufacturer, Manufactureraccessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)FQL1Contract manufacturer, Manufactureraccessdata.fda.gov
Support, HerniaEXN1Contract manufacturer, 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
July 10, 2008K080200WATER WORKS DOUCHING DEVICEHEDSubstantially EquivalentAbbott Research Group, Inc.accessdata.fda.gov
July 30, 1979K7911763M COLD/HOT WATER BAG AND WRAPFPFSubstantially Equivalent3M Companyaccessdata.fda.gov

Compare with other makers

Updated July 10, 2008. 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.