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Data / Medical devices / China / Shanghai Fimet Medical Instrument Co., Ltd.

Shanghai Fimet Medical Instrument Co., Ltd.: FDA-registered device maker in Shang hai Shanghai, China, 1 510(k) clearance

Shanghai Fimet Medical Instrument Co., Ltd. is registered with the FDA (registration 3008344699) in Shang hai Shanghai, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 1, 2005. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3008344699
Address
No.961, Kangqiao Road, Kangqiao Industrial Zone,Pudong New Area, Shang hai Shanghai, China, 200000
Owner or operator
Shanghai Fimet Medical Instrument Co., Ltd. (10088167)
Roles
Manufacturer
First device listed
June 6, 2023
Registered through
2026
Brand names listed
F1 Series Dental Chairs with Operative Unit

Devices it lists

DeviceProduct codeClassRoleSource
Unit, Operative DentalEIA1Manufactureraccessdata.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 1, 2005K052470F1 SERIES DENTAL CHAIRS WITH OPERATIVE UNITEIASubstantially EquivalentShanghai Fimet Medical Instrument Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 1, 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.