Identity
- Trade Name
- Ti-Core Flow Plus Sample FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- Core Material and Post Cement Syrangeable Dual Cure Natural Shade A2 Sample FDA UDI
- Model / Reference
- 832-01 FDA UDI
- Description
- Core Material and Post Cement Syrangeable Dual Cure Natural Shade A2 Sample FDA UDI
Identifiers
- Catalog Number
- 832-01 FDA UDI
- Primary DI / UDI-DI
- 00766054000204 FDA UDI
- 510(k) Number
- K101504 FDA UDI
- FDA Product Code
- EMA FDA UDI
- GMDN Term
- Dental composite resin FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3275 FDA UDI
- Commercial Distribution
- Not 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
Ti-Core Flow Plus Sample by Essential Dental Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 bfe67b70-c27d-48a8-b8da-499a91c94f5d 39 fields · synced May 31, 2026