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Sign in to claim this brandTIDI PRODUCTS, LLC
United States·US-MF-000012287
Last updated September 17, 2026
What TIDI PRODUCTS, LLC makes
TIDI Products, LLC manufactures single-use medical drapes, wearable percutaneous catheter/tube holders, urological fluid funnels, multifunction body cushions, eye splash shields, portable radiation shielding panels, nurse call systems, and cast/bandage waterproof bathing covers. These products are designed for clinical and patient care settings to enhance safety, hygiene, and comfort during medical procedures and daily use.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The portfolio is regulated under U.S. medical device laws, with individual products authorised through the relevant FDA clearance or exemption pathways.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does TIDI Products, LLC manufacture?
TIDI Products, LLC specializes in single-use and reusable medical devices primarily for clinical and patient care. Their portfolio includes items like medical drapes for equipment/instruments, wearable holders for percutaneous catheters or tubes, urological fluid funnels, multifunction body cushions, eye splash shields, portable radiation shielding panels, nurse call systems, and waterproof bathing covers for casts or bandages. These products are designed to improve hygiene, safety, and patient comfort during medical procedures and daily use.
Where is TIDI Products, LLC based?
TIDI Products, LLC is based in the United States. The company operates within U.S. regulatory frameworks, including FDA oversight for its medical devices.
Which regulatory registries list TIDI Products, LLC’s devices?
TIDI Products, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorised for use in the U.S. under FDA regulations, ensuring transparency and traceability for healthcare providers and regulators.
How are TIDI Products, LLC’s devices classified under FDA regulations?
TIDI Products, LLC’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may qualify for exemptions from premarket notification (510(k)) requirements, while Class II devices require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway each device follows for authorisation.
Are TIDI Products, LLC’s devices authorised for use in the U.S.?
Individual devices from TIDI Products, LLC are authorised for use in the U.S. through pathways like FDA clearance or exemptions, depending on their classification. The company’s products comply with U.S. medical device laws, but authorisation is granted per device, not the entire portfolio. Always verify a specific product’s status in the FDA’s UDI database or other relevant registries.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 570, Enterprise Drive, Neenah, United States
- Website
- tidiproducts.com
- —
- —
- [email protected]
- Phone
- 1-920-751-4300 x 4009
- PRRC Contact
- Chris Rahn
- EUDAMED SRN
- US-MF-000012287
- FDA FEI Number
- 2182318
- DUNS Number
- —
Catalogue (2730)
Page 21 of 55| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tidi | 9210-250DSP | FDA UDI | Class I | Active |
| Tidi | 501 | FDA UDI | Class II | Unknown |
| TIDIShield | CFI-689 N/S | FDA UDI | Class II | Unknown |
| Tidi | 192 | FDA UDI | Class II | Unknown |
| TIDIShield | TIDIFS96 | FDA UDI | Class I | Active |
| Medi-INN | MI-100MILCDN | FDA UDI | Class II | Active |
| Gems | 32964 | FDA UDI | Class II | Unknown |
| Tidi | CFI-655 | FDA UDI | Class II | Active |
| Tidi | 6-SCB | FDA UDI | Class II | Unknown |
| Tidi | 32969 | FDA UDI | Class II | Unknown |
| Plan 1 Health | 01.60.70.10 | FDA UDI | Class I | Active |
| Tidi | 32721 | FDA UDI | Class II | Unknown |
| Tidi | 23292 | FDA UDI | Class II | Unknown |
| Tidi | 172-20 | FDA UDI | Class II | Unknown |
| Drapetech | 28383 | FDA UDI | Class II | Unknown |
| Tidi | 30941 | FDA UDI | Class II | Unknown |
| TIDIShield | 5514 | FDA UDI | Class II | Unknown |
| Zero Gravity | ZGM-6-5H | FDA UDI | Class I | Active |
| Tidi | 33129 | FDA UDI | Class II | Unknown |
| Tidi | 815-V | FDA UDI | Class II | Unknown |
| Grip-Lok | 3200S-NSB | FDA UDI | Class I | Active |
| Vital Care | 23744 | FDA UDI | Class II | Active |
| TIDIShield | 5464 | FDA UDI | Class II | Active |
| Zero Gravity | ZGAV-3XL | FDA UDI | Class I | Active |
| TIDIShield | CFI-743 N/S | FDA UDI | Class II | Unknown |
| Tidi | 33010 | FDA UDI | Class II | Unknown |
| Tidi | 126-SCB | FDA UDI | Class II | Unknown |
| Tidi | 32543 | FDA UDI | Class II | Unknown |
| Tidi | 301-UF | FDA UDI | Class II | Unknown |
| Air Techniques | 20927 | FDA UDI | Class I | Active |
| Tidi | 24494 | FDA UDI | Class II | Unknown |
| Tidi | 32140 | FDA UDI | Class II | Unknown |
| SteriGear | 27605 | FDA UDI | Class I | Unknown |
| TIDIShield | 9112 | FDA UDI | Class II | Unknown |
| Medi-Inn | MICK-0024 | FDA UDI | Class II | Unknown |
| TIDIShield | 5427 | FDA UDI | Class II | Unknown |
| Bone Foam | 26032 | FDA UDI | Class II | Unknown |
| Tidi | 25354 | FDA UDI | Class II | Unknown |
| Tidishield | 21038 | FDA UDI | Class I | Active |
| Zero Gravity | ZGHH-CM48 | FDA UDI | Class I | Active |
| Grip-Lok | 3304MCS-BA | FDA UDI | Class I | Active |
| JAC-CELL Medic | 31812 | FDA UDI | Class II | Unknown |
| Tidi | 129-8 | FDA UDI | Class II | Unknown |
| Ziehm Imaging | 30896 | FDA UDI | Class II | Unknown |
| Dentrix | 20955 | FDA UDI | Class I | Active |
| Tidishield | 21106 | FDA UDI | Class II | Active |
| TIDIShield | CFI-893 | FDA UDI | Class II | Unknown |
| Tidi | 28524 | FDA UDI | Class I | Unknown |
| SteriGear | 27406 | FDA UDI | Class II | Unknown |
| Tidi | 26490 | FDA UDI | Class II | Unknown |
Related Companies
Authorised Representatives
- MDSS GmbH DE
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
TIDI Products, LLC has one FDA recall record initiated on April 12, 2019, which is listed with a terminated status. The recall was due to products not meeting design specifications.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 12, 2019 | Z-0194-2020 | — | terminated | Not meeting design specifications. |