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Data / Medical devices / United States / Tidi Products, LLC

Tidi Products, LLC: FDA-registered device maker in Neenah, WI, United States, 5 510(k) clearances

Tidi Products, LLC is registered with the FDA (registration 2182318) in Neenah, WI, United States. It lists 46 device types. The FDA files 5 510(k) clearances under its listings, the newest dated February 18, 2014. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2182318
Address
570 Enterprise Dr, Neenah, WI, United States, 54956
Owner or operator
TIDI PRODUCTS, LLC (9921057)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer
First device listed
July 16, 1992
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Absorber, Saliva, PaperKHR1Manufactureraccessdata.fda.gov
Accessory, Surgical ApparelLYU1Manufacturer, Specification developeraccessdata.fda.gov
Aid, TransferIKX1Specification developeraccessdata.fda.gov
Apron, LeadedEAJ1Specification developeraccessdata.fda.gov
Bag, Urine Collection, Leg, For External Use, Non-SterileNNW1Specification developeraccessdata.fda.gov
Bed, Ac-Powered Adjustable HospitalFNL2Specification developeraccessdata.fda.gov
Bedding, Disposable, MedicalKME1Manufacturer, Specification developeraccessdata.fda.gov
Camera, Surgical And AccessoriesKQM1Contract manufacturer, Manufacturer, Specification developeraccessdata.fda.gov
Cannula, Nasal, OxygenCAT1Manufactureraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Manufactureraccessdata.fda.gov
Cotton, RollEFN1Specification developeraccessdata.fda.gov
Cover, CastKIA1Specification developeraccessdata.fda.gov
Cuff, Tracheal Tube, InflatableBSK2Repackager or relabeleraccessdata.fda.gov
Dental Barriers And SleevesPEM2Contract manufacturer, Manufactureraccessdata.fda.gov
Device, Fixation, Tracheal TubeCBH1Specification developeraccessdata.fda.gov
Device, Intravascular Catheter SecurementKMK1Contract manufacturer, Manufacturer, Specification developeraccessdata.fda.gov
Drape, Surgical, ExemptPUI2Specification developeraccessdata.fda.gov
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Contract manufactureraccessdata.fda.gov
Fall Prevention Alarm/Sensor Attached OnlyPJP1Specification developeraccessdata.fda.gov
Fall Prevention Alarm/Sensor Combination Attached Or UnattachedPJO1Specification developeraccessdata.fda.gov
Fiber, Medical, AbsorbentFRL1Manufactureraccessdata.fda.gov
Garment, Protective, For IncontinenceEYQ1Specification developeraccessdata.fda.gov
Gastrointestional Tube HolderPLI2Manufactureraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Manufacturer, Specification developeraccessdata.fda.gov
Gown, ExaminationFME1Manufacturer, Specification developeraccessdata.fda.gov
Holder, Film, X-RayEGZ1Contract manufacturer, Manufactureraccessdata.fda.gov
Holder, Ureteral CatheterEYJ1Contract manufacturer, Manufactureraccessdata.fda.gov
Laryngoscope, RigidCCW1Contract manufactureraccessdata.fda.gov
Monitor, Bed PatientKMI1Manufacturer, Specification developeraccessdata.fda.gov
Non-Surgical GownOEA1Manufacturer, Specification developeraccessdata.fda.gov
Orthosis, Limb BraceIQI1Specification developeraccessdata.fda.gov
Pad, Neonatal EyeFOK1Specification developeraccessdata.fda.gov
Patient Bed With Canopy/RestraintsOYS1Manufactureraccessdata.fda.gov
Powered Microneedle DeviceQAI2Contract manufactureraccessdata.fda.gov
Protector, Skin PressureFMP1Specification developeraccessdata.fda.gov
Restraint, ProtectiveFMQ1Specification developeraccessdata.fda.gov
Scalpel, One-PieceGDX1Specification developeraccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Specification developeraccessdata.fda.gov
System, Imaging, Pulsed Echo, UltrasonicIYO2Contract manufacturer, Specification developeraccessdata.fda.gov
Table And Attachments, Operating-RoomBWN1Specification developeraccessdata.fda.gov
Table, Cystometric, ElectricMMZ2Specification developeraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Manufactureraccessdata.fda.gov
Toothbrush, PoweredJEQ1Contract manufactureraccessdata.fda.gov
Unit, Operative DentalEIA1Contract manufactureraccessdata.fda.gov
Unit, Syringe, Air And/Or WaterECB1Manufactureraccessdata.fda.gov
Wrap, SterilizationFRG2Manufactureraccessdata.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
February 18, 2014K132953TIDISHEILDPEMSubstantially EquivalentTidi Products,Llcaccessdata.fda.gov
September 18, 2009K090773CFI ULTRASOUND PROBE DRAPEIYOSubstantially EquivalentContour Fabricators, Inc.accessdata.fda.gov
November 17, 2004K042580TIDI BRAND STERILIZATION WRAPFRGSubstantially EquivalentBanta Healthcare Group, Ltd.accessdata.fda.gov
October 19, 1998K983406SANITHERM ORAL DISPOSABLE THERMOMETER SHEATHS FOR MERCURY THERMOMETER, SENITHERM ORAL DISPOSABLE THERMOMETER SHEATHS FORFLLSubstantially EquivalentBanta Healthcare Group, Ltd.accessdata.fda.gov
July 20, 1991K912723POSEY CUFFLATORBSKSubstantially EquivalentPosey Co.accessdata.fda.gov

Compare with other makers

Updated February 18, 2014. 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.