Tidi Products, LLC
Neenah, WI, US
TIDI PRODUCTS, LLC appears in FDA device records in Neenah, WI. FDA records list 3 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show one recall for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 3 510(k) clearances for Tidi Products, LLC between 2010 and 2014. The busiest year on record is 2010, with 2. The most recent is 2014, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2010 | 2 |
| 2014 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 2182318 | 2182318 | TIDI PRODUCTS, LLC | 570 Enterprise Dr, NEENAH, WI 54956 US | 2026 | and 36 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KHRAbsorber, Saliva, Paper
- LYUAccessory, Surgical Apparel
- IKXAid, Transfer
- EAJApron, Leaded
- NNWBag, Urine Collection, Leg, For External Use, Non-Sterile
- FNLBed, Ac-Powered Adjustable Hospital
- KMEBedding, Disposable, Medical
- KQMCamera, Surgical And Accessories
- CATCannula, Nasal, Oxygen
- FLLContinuous Measurement Thermometer
- EFNCotton, Roll
- KIACover, Cast
- BSKCuff, Tracheal Tube, Inflatable
- PEMDental Barriers And Sleeves
- CBHDevice, Fixation, Tracheal Tube
- KMKDevice, Intravascular Catheter Securement
- PUIDrape, Surgical, Exempt
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- PJPFall Prevention Alarm/Sensor Attached Only
- PJOFall Prevention Alarm/Sensor Combination Attached Or Unattached
- FRLFiber, Medical, Absorbent
- EYQGarment, Protective, For Incontinence
- PLIGastrointestional Tube Holder
- NABGauze / Sponge,Nonresorbable For External Use
- FMEGown, Examination
- EGZHolder, Film, X-Ray
- EYJHolder, Ureteral Catheter
- CCWLaryngoscope, Rigid
- FXXMask, Surgical
- KMIMonitor, Bed Patient
- OEANon-Surgical Gown
- IQIOrthosis, Limb Brace
- FOKPad, Neonatal Eye
- OYSPatient Bed With Canopy/Restraints
- QAIPowered Microneedle Device
- FMPProtector, Skin Pressure
- FMQRestraint, Protective
- GDXScalpel, One-Piece
- NOCSplint, Extremity, Non-Inflatable, External, Non-Sterile
- IYOSystem, Imaging, Pulsed Echo, Ultrasonic
- BWNTable And Attachments, Operating-Room
- MMZTable, Cystometric, Electric
- KGXTape And Bandage, Adhesive
- JEQToothbrush, Powered
- EIAUnit, Operative Dental
- ECBUnit, Syringe, Air And/Or Water
- FRGWrap, Sterilization
Recall records
| Recall | Product | Reason | Classification | Initiated | Status |
|---|---|---|---|---|---|
| Z-0194-2020 | Posey Connected Twice-As-Tough Cuffs | Not meeting design specifications. | Class II | Terminated |
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain