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Data / Medical devices / China / Guangdong Jinme Medical Technology Co., Ltd.

Guangdong Jinme Medical Technology Co., Ltd.: FDA-registered device maker in Foshan Guangdong, China, 4 510(k) clearances

Guangdong Jinme Medical Technology Co., Ltd. is registered with the FDA (registration 3012336822) in Foshan Guangdong, China. It lists 13 device types. The FDA files 4 510(k) clearances under its listings, the newest dated November 13, 2024. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012336822
Address
No.301,401,501 of Building 3, Wanyang Kexing Park, No. 84 Taoyuan East Road, Shishan Town, Nanhai District, Foshan Guangdong, China, 528225
Owner or operator
Guangdong JINME Medical Technology Co., Ltd. (10051074)
Roles
Manufacturer
First device listed
January 10, 2018
Registered through
2026
Brand names listed
Air compressor (model: Air compressor), Dental Burs, Dental Handpiece (Model: J6-126, J6-136, SH11W2, SH11W3, W401LW, W15LW, W142LW, W11L), Dental High-Speed Turbine Handpiece (Model: T, S, TU, SU, TP, SP, TUQ, TUP, SUP, SUQ, TUQP, SUQP), Dental Low-Speed Turbine Handpiece (Model: LN, L), Dental air compressor, Dental chair and accessories (Model: S600, S690, S610), Intra Oral Camera (Model: ECO-CAMERA 01, ECO-CAMERA 02, ECO-CAMERA 03) 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
November 13, 2024K240337Dental Handpiece (Model: J6-126, J6-136, SH11W2, SH11W3, W401LW, W15LW, W142LW, W11L)EFBSubstantially EquivalentGuangdong Jinme Medical Technology Co., Ltd.accessdata.fda.gov
July 18, 2024K240340Surgical Drive System (Model: ES70, ES90, E8)DZISubstantially EquivalentGuangdong Jinme Medical Technology Co., Ltd.accessdata.fda.gov
November 21, 2017K170236Dental Low-speed Turbine HandpieceEFBSubstantially EquivalentGuangdong Jinme Medical Technology Co., Ltd.accessdata.fda.gov
November 8, 2017K170229Dental High-speed Turbine HandpieceEFBSubstantially EquivalentGuangdong Jinme Medical Technology Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated November 13, 2024. 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.