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Innovative Medical Manufacturing Co.: FDA-registered device maker in Zhunan Township, Miaoli County, Taiwan, 1 510(k) clearance

Innovative Medical Manufacturing Co. is registered with the FDA (registration 3003974574) in Zhunan Township, Miaoli County, Taiwan. It lists 17 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 24, 2007. Registered through 2027. FDA data exported November 2, 2026.

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Get makers like this oneWatch Innovative Medical Manufacturing Co.
FDA registration number
3003974574
Address
No. 107, LN 181, SEC 1, Yongzhen Rd., Zhunan Township, Miaoli County, Taiwan, 35057
Owner or operator
INNOVATIVE MEDICAL MANUFACTURING CO. (9076256)
Roles
Complaint file establishment, Contract manufacturer, Contract sterilizer, Manufacturer
First device listed
August 10, 2005
Registered through
2027
Brand names listed
"IMM" Hypodermic needle set, "Puriblood" Leukocyte Reduction Filtration System for Red Blood Cells, Blunt Cannula Assembly, Gastroenterology/Urology, URINARY CATHETER, Intravenous Tubing Set, Needleless access device, PAV luer lock device, Urinary Catheter and more

Devices it lists

DeviceProduct codeClassRoleSource
Adaptor, CatheterGCE1Contract manufacturer, Contract sterilizeraccessdata.fda.gov
Applicator, VaginalHGD1Contract manufactureraccessdata.fda.gov
Catheter, CoudeEZC2Contract manufactureraccessdata.fda.gov
Catheter, IrrigationGBX1Manufactureraccessdata.fda.gov
Catheter, StraightEZD2Contract manufactureraccessdata.fda.gov
Container, Empty, For Collection & Processing Of Blood & Blood ComponentsKSR2Contract manufacturer, Contract sterilizeraccessdata.fda.gov
CuretteHTF1Complaint file establishment, Contract manufacturer, Contract sterilizeraccessdata.fda.gov
Device, Intravascular Catheter SecurementKMK1Contract manufacturer, Contract sterilizeraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Contract manufacturer, Contract sterilizeraccessdata.fda.gov
EsthesiometerGXB1Contract manufactureraccessdata.fda.gov
Introducer, Syringe NeedleKZH2Contract manufactureraccessdata.fda.gov
Needle, Hypodermic, Single LumenFMI2Contract manufactureraccessdata.fda.gov
Set, Administration, IntravascularFPA2Contract manufacturer, Contract sterilizer, Manufactureraccessdata.fda.gov
Set, I.V. Fluid TransferLHI2Contract manufactureraccessdata.fda.gov
Syringe, PistonFMF2Contract manufactureraccessdata.fda.gov
Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA2Contract manufactureraccessdata.fda.gov
Tubing, Fluid DeliveryFPK2Contract 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
May 24, 2007K070801IMM HYPODERMIC NEEDLE SETFPASubstantially EquivalentInnovative Medical Manufacturing Co.accessdata.fda.gov

Compare with other makers

Updated May 24, 2007. 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.