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Tops Medical Articles Industries Nantong Inc: FDA-registered device maker in Qidong City Jiangsu, China, 1 510(k) clearance

Tops Medical Articles Industries Nantong Inc is registered with the FDA (registration 3004615451) in Qidong City Jiangsu, China. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 3, 1982. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
3004615451
Address
South Hezoucaojia Town, Qidong City Jiangsu, China, 226215
Owner or operator
Tops Medical Articles Industries Nantong Inc (9064964)
Roles
Contract manufacturer, Manufacturer
First device listed
July 14, 2004
Registered through
2026
Brand names listed
Apex, Arm Sling, RTL,1EA,6/CS, BBF Hot and Cold Pack, COMPASS HEALTH BRANDS, CRX EZ CAST PROTECT-LEG, CVS Reusable Cold Pack, Carex, Cast Protector, Arm and more

Devices it lists

DeviceProduct codeClassRoleSource
Aid, TransferIKX1Contract manufacturer, Manufactureraccessdata.fda.gov
Attachment, Commode, WheelchairINB1Contract manufacturer, Manufactureraccessdata.fda.gov
Bag, IceKYR1Contract manufacturer, Manufactureraccessdata.fda.gov
Bandage, Liquid, Skin ProtectantNEC1Contract manufacturer, Manufactureraccessdata.fda.gov
Bottle, Hot/Cold WaterFPF1Contract manufacturer, Manufactureraccessdata.fda.gov
Cover, CastKIA1Contract manufacturer, Manufactureraccessdata.fda.gov
Cushion, FlotationKIC1Contract manufacturer, Manufactureraccessdata.fda.gov
Cushion, WheelchairIMP1Contract manufacturer, Manufactureraccessdata.fda.gov
Dispenser, Solid MedicationNXB1Contract manufacturer, Manufactureraccessdata.fda.gov
Lift, Patient, Non-Ac-PoweredFSA1Contract manufacturer, Manufactureraccessdata.fda.gov
Orthosis, CervicalIQK1Contract manufacturer, Manufactureraccessdata.fda.gov
Orthosis, LumbarIQE1Contract manufacturer, Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Manufactureraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Manufactureraccessdata.fda.gov
Sling, ArmILI1Contract manufacturer, Manufactureraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Manufactureraccessdata.fda.gov
Strap, Head, Gas MaskBTK1Contract manufacturer, Manufactureraccessdata.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 3, 1982K823393STAX FINGER SPLINTSILHSubstantially EquivalentOrthopedic Systems, Inc.accessdata.fda.gov

Compare with other makers

Updated December 3, 1982. 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.