Identity
- Trade Name
- Ti-Core Flow Plus FDA UDI
- Generic Name
- Custom-made dental composite resin kit FDA UDI
- Device Name
- Core Material and Post Cement Syrangeable Dual Cure Natural Shade A2 FDA UDI
- Model / Reference
- 832-00 FDA UDI
- Description
- Core Material and Post Cement Syrangeable Dual Cure Natural Shade A2 FDA UDI
Identifiers
- Catalog Number
- 832-00 FDA UDI
- Primary DI / UDI-DI
- 00766054000051 FDA UDI
- 510(k) Number
- K101504 FDA UDI
- FDA Product Code
- EMA FDA UDI
- GMDN Term
- Custom-made dental composite resin kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3275 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
FDA UDI
Category: Custom-made dental composite resin kit
Ti-Core Flow Plus by Essential Dental Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K101504 also covers:
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
- Essential Dental Systems, Inc.
Sources (1)
- FDA UDI 5c2fc597-dfc4-4ec9-ac98-de22238f13c7 38 fields · synced May 30, 2026