Identity
- Trade Name
- Core-Flo DC Lite FDA UDI
- Generic Name
- Dental composite resin FDA UDI
- Device Name
- Core-Flo DC Lite 2g Natural A1 Pkg FDA UDI
- Model / Reference
- A-17801SP FDA UDI
- Description
- Core-Flo DC Lite 2g Natural A1 Pkg FDA UDI
Identifiers
- Catalog Number
- A-17801SP FDA UDI
- Primary DI / UDI-DI
- D757A17801SP1 FDA UDI
- FDA Product Code
- EID FDA UDIEBF FDA UDI
- GMDN Term
- Dental composite resin FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI872.3690 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
Core-Flo DC Lite by Bisco Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Bisco Inc.
Sources (1)
- FDA UDI bffe41cb-43e2-4bcd-af4e-345ee7ed693f 37 fields · synced May 30, 2026