Identity
- Trade Name
- SILJET FDA UDI
- Generic Name
- Dental porcelain/ceramic restoration kit FDA UDI
- Device Name
- SILJET,POWDER,REFILL,(3) FDA UDI
- Model / Reference
- 93596 FDA UDI
- Description
- SILJET,POWDER,REFILL,(3) FDA UDI
Identifiers
- Catalog Number
- 93596 FDA UDI
- Primary DI / UDI-DI
- 00816594021853 FDA UDI
- FDA Product Code
- EBF FDA UDI
- GMDN Term
- Dental porcelain/ceramic restoration kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3690 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: Dental porcelain/ceramic restoration kit
Siljet by Danville Materials, Llc — 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
- Danville Materials, Llc
Sources (1)
- FDA UDI 29ce52a0-97d4-4b6b-b12a-9ddaae6e8c0a 36 fields · synced May 31, 2026