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Data / Medical devices / China / Shanghai SA Medical & Plastic Instruments Co., Ltd.

Shanghai SA Medical & Plastic Instruments Co., Ltd.: FDA-registered device maker in Shanghai, China, 1 510(k) clearance

Shanghai SA Medical & Plastic Instruments Co., Ltd. is registered with the FDA (registration 3007421133) in Shanghai, China. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 21, 2012. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3007421133
Address
Building No.12,No.2755 Sanlu Highway,Minhang District, Shanghai, China, 201112
Owner or operator
Shanghai SA Medical & Plastic Instruments Co., Ltd. (10027851)
Roles
Manufacturer
First device listed
May 7, 2018
Registered through
2026
Brand names listed
ANESTHESIA CONDUCTION NEEDLES

Devices it lists

DeviceProduct codeClassRoleSource
Needle, Conduction, Anesthetic (W/Wo Introducer)BSP2Manufactureraccessdata.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
December 21, 2012K120475ANESTHESIA CONDUCTION NEEDLESBSPSubstantially EquivalentShanghai Samedical & Plastic Instruments Co., Ltd.accessdata.fda.gov

Compare with other makers

Updated December 21, 2012. 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.