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Data / Medical devices / Taiwan / Fego Precision Industrial Co., Ltd.

Fego Precision Industrial Co., Ltd.: FDA-registered device maker in Taichung City, Taiwan, 1 510(k) clearance

Fego Precision Industrial Co., Ltd. is registered with the FDA (registration 3007353620) in Taichung City, Taiwan. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 8, 2007. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
3007353620
Address
947 Lin-Sen Rd. Wu-Fong Dist, Taichung City, Taiwan, 413
Owner or operator
Fego Precision Industrial Co., Ltd. (10027447)
Roles
Contract manufacturer, Manufacturer
First device listed
November 10, 2008
Registered through
2027
Brand names listed
Body Furance #06200

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
August 8, 2007K070209FB-100U SERIES DIGITAL BLOOD PRESSURE MONITORDXNSubstantially EquivalentFego Precision Industrial Co;, Ltd.accessdata.fda.gov

Compare with other makers

Updated August 8, 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.