Identity
- Trade Name
- Tangible Boost FDA UDI
- Generic Name
- Contact lens rinsing solution FDA UDI
- Device Name
- Tangible Boost is a monthly treatment to restore the Tangible Hydra-PEG® coating, and maintain the wettability of Tangible Hydra-PEG coated fluorosilicone acrylate rigid gas permeable lenses. Tangible Boost is intended for prescription (Rx) use only. FDA UDI
- Model / Reference
- A FDA UDI
- Description
- Tangible Boost is a monthly treatment to restore the Tangible Hydra-PEG® coating, and maintain the wettability of Tangible Hydra-PEG coated fluorosilicone acrylate rigid gas permeable lenses. Tangible Boost is intended for prescription (Rx) use only. FDA UDI
Identifiers
- Catalog Number
- FG6 FDA UDI
- Primary DI / UDI-DI
- B673FG6 FDA UDI
- 510(k) Number
- DEN200002 FDA UDI
- FDA Product Code
- QMM FDA UDI
- GMDN Term
- Contact lens rinsing solution FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.5919 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Contact lens rinsing solution
Tangible Boost by TANGIBLE SCIENCE Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- TANGIBLE SCIENCE Inc
Sources (1)
- FDA UDI 7d934724-03a7-44a2-bdad-ec6bba12d404 36 fields · synced May 30, 2026