Identity
- Trade Name
- Bioform® VF 20 Deg. Porcelain Posteriors FDA UDI
- Generic Name
- Ceramic artificial teeth FDA UDI
- Model / Reference
- B77 U 31S FDA UDI
Identifiers
- Catalog Number
- 13563 FDA UDI
- Primary DI / UDI-DI
- D00113563UB7731S0 FDA UDI
- FDA Product Code
- ELL FDA UDI
- GMDN Term
- Ceramic artificial teeth FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3920 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Bioform® VF 20 Deg. Porcelain Posteriors by Dentsply International — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Dentsply International
Sources (1)
- FDA UDI 58fca500-0589-417e-9328-5f45c28d1787 35 fields · synced May 31, 2026