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
| Device | Product code | Class | Role | Source |
|---|
| Absorber, Saliva, Paper | KHR | 1 | Manufacturer | accessdata.fda.gov |
| Accessory, Surgical Apparel | LYU | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Aid, Transfer | IKX | 1 | Specification developer | accessdata.fda.gov |
| Apron, Leaded | EAJ | 1 | Specification developer | accessdata.fda.gov |
| Bag, Urine Collection, Leg, For External Use, Non-Sterile | NNW | 1 | Specification developer | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Specification developer | accessdata.fda.gov |
| Bedding, Disposable, Medical | KME | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Camera, Surgical And Accessories | KQM | 1 | Contract manufacturer, Manufacturer, Specification developer | accessdata.fda.gov |
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Manufacturer | accessdata.fda.gov |
| Cotton, Roll | EFN | 1 | Specification developer | accessdata.fda.gov |
| Cover, Cast | KIA | 1 | Specification developer | accessdata.fda.gov |
| Cuff, Tracheal Tube, Inflatable | BSK | 2 | Repackager or relabeler | accessdata.fda.gov |
| Dental Barriers And Sleeves | PEM | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Device, Fixation, Tracheal Tube | CBH | 1 | Specification developer | accessdata.fda.gov |
| Device, Intravascular Catheter Securement | KMK | 1 | Contract manufacturer, Manufacturer, Specification developer | accessdata.fda.gov |
| Drape, Surgical, Exempt | PUI | 2 | Specification developer | accessdata.fda.gov |
| Electrosurgical, Cutting & Coagulation & Accessories | GEI | 2 | Contract manufacturer | accessdata.fda.gov |
| Fall Prevention Alarm/Sensor Attached Only | PJP | 1 | Specification developer | accessdata.fda.gov |
| Fall Prevention Alarm/Sensor Combination Attached Or Unattached | PJO | 1 | Specification developer | accessdata.fda.gov |
| Fiber, Medical, Absorbent | FRL | 1 | Manufacturer | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Specification developer | accessdata.fda.gov |
| Gastrointestional Tube Holder | PLI | 2 | Manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Gown, Examination | FME | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Holder, Film, X-Ray | EGZ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Holder, Ureteral Catheter | EYJ | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Contract manufacturer | accessdata.fda.gov |
| Monitor, Bed Patient | KMI | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 1 | Manufacturer, Specification developer | accessdata.fda.gov |
| Orthosis, Limb Brace | IQI | 1 | Specification developer | accessdata.fda.gov |
| Pad, Neonatal Eye | FOK | 1 | Specification developer | accessdata.fda.gov |
| Patient Bed With Canopy/Restraints | OYS | 1 | Manufacturer | accessdata.fda.gov |
| Powered Microneedle Device | QAI | 2 | Contract manufacturer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Specification developer | accessdata.fda.gov |
| Restraint, Protective | FMQ | 1 | Specification developer | accessdata.fda.gov |
| Scalpel, One-Piece | GDX | 1 | Specification developer | accessdata.fda.gov |
| Splint, Extremity, Non-Inflatable, External, Non-Sterile | NOC | 1 | Specification developer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Contract manufacturer, Specification developer | accessdata.fda.gov |
| Table And Attachments, Operating-Room | BWN | 1 | Specification developer | accessdata.fda.gov |
| Table, Cystometric, Electric | MMZ | 2 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Manufacturer | accessdata.fda.gov |
| Toothbrush, Powered | JEQ | 1 | Contract manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 1 | Contract manufacturer | accessdata.fda.gov |
| Unit, Syringe, Air And/Or Water | ECB | 1 | Manufacturer | accessdata.fda.gov |
| Wrap, Sterilization | FRG | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|
| February 18, 2014 | K132953 | TIDISHEILD | PEM | Substantially Equivalent | Tidi Products,Llc | accessdata.fda.gov |
| September 18, 2009 | K090773 | CFI ULTRASOUND PROBE DRAPE | IYO | Substantially Equivalent | Contour Fabricators, Inc. | accessdata.fda.gov |
| November 17, 2004 | K042580 | TIDI BRAND STERILIZATION WRAP | FRG | Substantially Equivalent | Banta Healthcare Group, Ltd. | accessdata.fda.gov |
| October 19, 1998 | K983406 | SANITHERM ORAL DISPOSABLE THERMOMETER SHEATHS FOR MERCURY THERMOMETER, SENITHERM ORAL DISPOSABLE THERMOMETER SHEATHS FOR | FLL | Substantially Equivalent | Banta Healthcare Group, Ltd. | accessdata.fda.gov |
| July 20, 1991 | K912723 | POSEY CUFFLATOR | BSK | Substantially Equivalent | Posey 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.