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Data / Medical devices / China / Shanghai Wilpower Industrial Co., Ltd

Shanghai Wilpower Industrial Co., Ltd: FDA-registered device maker in Shanghai, China, 1 510(k) clearance

Shanghai Wilpower Industrial Co., Ltd is registered with the FDA (registration 3009865268) in Shanghai, China. It lists 33 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 7, 1994. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Shanghai Wilpower Industrial Co., Ltd
FDA registration number
3009865268
Address
20/F, 1958 Zhong Shan North Road, Shanghai, China, 200063
Owner or operator
SHANGHAI WILPOWER INDUSTRIAL CO., LTD (10089807)
Roles
Exporter to the US
First device listed
January 9, 2024
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Attachment, Commode, WheelchairINB1Exporter to the USaccessdata.fda.gov
Bandage, CastITG1Exporter to the USaccessdata.fda.gov
Bandage, ElasticFQM1Exporter to the USaccessdata.fda.gov
Bit, DrillHTW1Exporter to the USaccessdata.fda.gov
Bur, Surgical, General & Plastic SurgeryGFF1Exporter to the USaccessdata.fda.gov
ClampHXD1Exporter to the USaccessdata.fda.gov
Clamp, Surgical, General & Plastic SurgeryGDJ1Exporter to the USaccessdata.fda.gov
Components, WheelchairKNN1Exporter to the USaccessdata.fda.gov
Depressor, Tongue, Non-SurgicalFMA1Exporter to the USaccessdata.fda.gov
Device, Monitoring, Intracranial PressureGWM2Exporter to the USaccessdata.fda.gov
Drills, Burrs, Trephines & Accessories (Manual)HBG2Exporter to the USaccessdata.fda.gov
Footrest, WheelchairIMM1Exporter to the USaccessdata.fda.gov
ForcepsHTD1Exporter to the USaccessdata.fda.gov
Forceps, Biopsy, Non-ElectricFCL1Exporter to the USaccessdata.fda.gov
Forceps, General & Plastic SurgeryGEN1Exporter to the USaccessdata.fda.gov
Guide, Needle, SurgicalGDF1Exporter to the USaccessdata.fda.gov
Handle, ScalpelGDZ1Exporter to the USaccessdata.fda.gov
HemostatHRQ1Exporter to the USaccessdata.fda.gov
Instrument, Manual, General Obstetric-GynecologicKOH1Exporter to the USaccessdata.fda.gov
Instrument, Surgical, Non-PoweredHAO1Exporter to the USaccessdata.fda.gov
Joint, Hip, External Limb ComponentISL1Exporter to the USaccessdata.fda.gov
Marker, SkinFZZ1Exporter to the USaccessdata.fda.gov
RetractorGAD1Exporter to the USaccessdata.fda.gov
Retractor, EntKAL1Exporter to the USaccessdata.fda.gov
Retractor, Non-Self-RetainingFGN1Exporter to the USaccessdata.fda.gov
Retractor, VaginalHDL1Exporter to the USaccessdata.fda.gov
Scissors, EpisiotomyHDK1Exporter to the USaccessdata.fda.gov
Scissors, General, SurgicalLRW1Exporter to the USaccessdata.fda.gov
Scissors, NasalKBD1Exporter to the USaccessdata.fda.gov
Scissors, OphthalmicHNF1Exporter to the USaccessdata.fda.gov
Scissors, UmbilicalHDJ1Exporter to the USaccessdata.fda.gov
Speculum, Vaginal, MetalHDF1Exporter to the USaccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Exporter to the USaccessdata.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
March 7, 1994K914479MICROSENSOR INTRACRANIAL PRESSURE TRANSDUCERGWMSubstantially EquivalentCodman & Shurtleff, Inc.accessdata.fda.gov

Compare with other makers

Updated March 7, 1994. 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.