Skip to the page

Data / Medical devices / Taiwan / Fa Horn Trading Incorporated Company

Fa Horn Trading Incorporated Company: FDA-registered device maker in JIAYI COUNTY Chiayi(City), Taiwan, 2 510(k) clearances

Fa Horn Trading Incorporated Company is registered with the FDA (registration 3021327432) in JIAYI COUNTY Chiayi(City), Taiwan. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 9, 2005. Registered through 2026. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3021327432
Address
No. 1, BENTING BENCUO VILLAGE, XIKOU TOWNSHIP, JIAYI COUNTY Chiayi(City), Taiwan, 62348
Owner or operator
TAIWAN AN I CO.,LTD. (9021165)
Roles
Manufacturer
First device listed
March 27, 2002
Registered through
2026
Brand names listed
AMG USA, Airgo, Alevo, Barton Medical Corporation, Breezy, Drive, Feather, GF and more

Devices it lists

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
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
February 15, 2001K010094A & I WHEELCHAIRSIORSubstantially EquivalentTaiwan an I Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 9, 2005. 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.